Canonical Allele Identifier: CA399701109

Gene: SOST

Linked Data

• dbSNP Id: rs1974115237
• MyVariant Identifiers: chr17:g.41832711T>C (hg19) ; chr17:g.43755343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755343T>C , CM000679.2:g.43755343T>C	GRCh38
NC_000017.10:g.41832711T>C , CM000679.1:g.41832711T>C	GRCh37
NC_000017.9:g.39188237T>C	NCBI36
NG_008078.2:g.8446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.641A>G MANE Select	ENSP00000301691.1:p.Ter214Trp
ENST00000301691.2:c.641A>G	ENSP00000301691.1:p.Ter214Trp
NM_025237.2:c.641A>G	NP_079513.1:p.Ter214Trp
NM_025237.3:c.641A>G MANE Select	NP_079513.1:p.Ter214Trp