Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 11:57602081 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 14193

This variation has 20 HGVS names - click the plus to show

11:g.57602081C>G
ENST00000278407.6:c.597C>G
ENSP00000278407.4:p.Tyr199Ter
ENST00000531605.1:n.37C>G
ENST00000531797.3:c.98C>G
ENSP00000432554.1:p.Thr33Ser
ENST00000403558.1:c.699C>G
ENSP00000384420.1:p.Tyr233Ter
ENST00000619430.1:c.348+1906C>G
ENST00000378324.4:c.441C>G
ENSP00000367575.2:p.Tyr147Ter
ENST00000340687.8:c.597C>G
ENSP00000341861.6:p.Tyr199Ter
ENST00000531133.3:c.98C>G
ENSP00000435431.1:p.Thr33Ser
ENST00000378323.6:c.612C>G
ENSP00000367574.4:p.Tyr204Ter
LRG_105:g.9528C>G
LRG_105t1.1:c.597C>G
LRG_105p1.1:p.Tyr199Ter

Variation displays