Canonical Allele Identifier: CA399702146
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs762778690

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755649G>A , CM000679.2:g.43755649G>A GRCh38
NC_000017.10:g.41833017G>A , CM000679.1:g.41833017G>A GRCh37
NC_000017.9:g.39188543G>A NCBI36
NG_008078.2:g.8140C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.335C>T MANE Select ENSP00000301691.1:p.Ala112Val
ENST00000301691.2:c.335C>T ENSP00000301691.1:p.Ala112Val
NM_025237.2:c.335C>T NP_079513.1:p.Ala112Val
NM_025237.3:c.335C>T MANE Select NP_079513.1:p.Ala112Val