Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 7:114662075 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012948

Most severe consequence
Clinical significance

Synonyms

LSDB 13111

This variation has 17 HGVS names - click the plus to show

7:g.114662075G>A
ENST00000441290.4:c.*1658G>A
ENST00000393489.5:c.1382G>A
ENSP00000377129.3:p.Arg461His
ENST00000408937.5:c.1733G>A
ENSP00000386200.3:p.Arg578His
ENST00000412402.3:c.*1376G>A
ENST00000393498.4:c.1595G>A
ENSP00000377135.2:p.Arg532His
ENST00000403559.6:c.1709G>A
ENSP00000385069.4:p.Arg570His
ENST00000393491.5:c.1103G>A
ENSP00000377130.3:p.Arg368His
ENST00000350908.6:c.1658G>A
ENSP00000265436.7:p.Arg553His
ENST00000393494.4:c.1658G>A
ENSP00000377132.2:p.Arg553His

Variation displays