Canonical Allele Identifier: CA290857230
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs955970822

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755773G>A , CM000679.2:g.43755773G>A GRCh38
NC_000017.10:g.41833141G>A , CM000679.1:g.41833141G>A GRCh37
NC_000017.9:g.39188667G>A NCBI36
NG_008078.2:g.8016C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-10C>T MANE Select ENSP00000301691.1:n.221-10C>T
ENST00000301691.2:c.221-10C>T ENSP00000301691.1:n.221-10C>T
NM_025237.2:c.221-10C>T NP_079513.1:n.221-10C>T
NM_025237.3:c.221-10C>T MANE Select NP_079513.1:n.221-10C>T