Canonical Allele Identifier: CA8592804
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs776585836

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755628A>C , CM000679.2:g.43755628A>C GRCh38
NC_000017.10:g.41832996A>C , CM000679.1:g.41832996A>C GRCh37
NC_000017.9:g.39188522A>C NCBI36
NG_008078.2:g.8161T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.356T>G MANE Select ENSP00000301691.1:p.Ile119Ser
ENST00000301691.2:c.356T>G ENSP00000301691.1:p.Ile119Ser
NM_025237.2:c.356T>G NP_079513.1:p.Ile119Ser
NM_025237.3:c.356T>G MANE Select NP_079513.1:p.Ile119Ser