Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 11:57614475 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 38 HGVS names - click the plus to show

Variant allele A
11:g.57614475G>A
ENST00000278407.6:c.1397G>A
ENSP00000278407.4:p.Arg466His
ENST00000528996.1:c.*337G>A
ENST00000531797.3:c.*422G>A
ENST00000403558.1:c.1526G>A
ENSP00000384420.1:p.Arg509His
ENST00000619430.1:c.*126G>A
ENST00000530113.1:n.854G>A
ENST00000378324.4:c.1241G>A
ENSP00000367575.2:p.Arg414His
ENST00000340687.8:c.1286G>A
ENSP00000341861.6:p.Arg429His
ENST00000531133.3:c.*766G>A
ENST00000378323.6:c.1412G>A
ENSP00000367574.4:p.Arg471His
LRG_105:g.21922G>A
LRG_105t1:c.1397G>A
LRG_105p1:p.Arg466His

Variant allele T
11:g.57614475G>T
ENST00000278407.6:c.1397G>T
ENSP00000278407.4:p.Arg466Leu
ENST00000528996.1:c.*337G>T
ENST00000531797.3:c.*422G>T
ENST00000403558.1:c.1526G>T
ENSP00000384420.1:p.Arg509Leu
ENST00000619430.1:c.*126G>T
ENST00000530113.1:n.854G>T
ENST00000378324.4:c.1241G>T
ENSP00000367575.2:p.Arg414Leu
ENST00000340687.8:c.1286G>T
ENSP00000341861.6:p.Arg429Leu
ENST00000531133.3:c.*766G>T
ENST00000378323.6:c.1412G>T
ENSP00000367574.4:p.Arg471Leu
LRG_105:g.21922G>T
LRG_105t1:c.1397G>T
LRG_105p1:p.Arg466Leu

Variation displays