Canonical Allele Identifier: CA399701201

Gene: SOST

Linked Data

• MyVariant Identifiers: chr17:g.41832736G>C (hg19) ; chr17:g.43755368G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43755368G>C , CM000679.2:g.43755368G>C	GRCh38
NC_000017.10:g.41832736G>C , CM000679.1:g.41832736G>C	GRCh37
NC_000017.9:g.39188262G>C	NCBI36
NG_008078.2:g.8421C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301691.3:c.616C>G MANE Select	ENSP00000301691.1:p.Gln206Glu
ENST00000301691.2:c.616C>G	ENSP00000301691.1:p.Gln206Glu
NM_025237.2:c.616C>G	NP_079513.1:p.Gln206Glu
NM_025237.3:c.616C>G MANE Select	NP_079513.1:p.Gln206Glu