Canonical Allele Identifier: CA8592763
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs767644132

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755392G>C , CM000679.2:g.43755392G>C GRCh38
NC_000017.10:g.41832760G>C , CM000679.1:g.41832760G>C GRCh37
NC_000017.9:g.39188286G>C NCBI36
NG_008078.2:g.8397C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.592C>G MANE Select ENSP00000301691.1:p.Arg198Gly
ENST00000301691.2:c.592C>G ENSP00000301691.1:p.Arg198Gly
NM_025237.2:c.592C>G NP_079513.1:p.Arg198Gly
NM_025237.3:c.592C>G MANE Select NP_079513.1:p.Arg198Gly