Canonical Allele Identifier: CA399701261

Gene: SOST

Linked Data

• dbSNP Id: rs769015314
• gnomAD v2: 17-41832754-G-C
• gnomAD v4: 17-43755386-G-C
• MyVariant Identifiers: chr17:g.41832754G>C (hg19) ; chr17:g.43755386G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755386G>C , CM000679.2:g.43755386G>C	GRCh38
NC_000017.10:g.41832754G>C , CM000679.1:g.41832754G>C	GRCh37
NC_000017.9:g.39188280G>C	NCBI36
NG_008078.2:g.8403C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.598C>G MANE Select	ENSP00000301691.1:p.Arg200Gly
ENST00000301691.2:c.598C>G	ENSP00000301691.1:p.Arg200Gly
NM_025237.2:c.598C>G	NP_079513.1:p.Arg200Gly
NM_025237.3:c.598C>G MANE Select	NP_079513.1:p.Arg200Gly