Canonical Allele Identifier: CA399701122

Gene: SOST

Linked Data

• MyVariant Identifiers: chr17:g.41832714T>G (hg19) ; chr17:g.43755346T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755346T>G , CM000679.2:g.43755346T>G	GRCh38
NC_000017.10:g.41832714T>G , CM000679.1:g.41832714T>G	GRCh37
NC_000017.9:g.39188240T>G	NCBI36
NG_008078.2:g.8443A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.638A>C MANE Select	ENSP00000301691.1:p.Tyr213Ser
ENST00000301691.2:c.638A>C	ENSP00000301691.1:p.Tyr213Ser
NM_025237.2:c.638A>C	NP_079513.1:p.Tyr213Ser
NM_025237.3:c.638A>C MANE Select	NP_079513.1:p.Tyr213Ser