Canonical Allele Identifier: CA2261069130
Gene: SOST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755397C= , CM000679.2:g.43755397C= GRCh38
NC_000017.10:g.41832765C= , CM000679.1:g.41832765C= GRCh37
NC_000017.9:g.39188291C= NCBI36
NG_008078.2:g.8392G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.587G= MANE Select ENSP00000301691.1:p.Arg196=
ENST00000301691.2:c.587G= ENSP00000301691.1:p.Arg196=
NM_025237.2:c.587G= NP_079513.1:p.Arg196=
NM_025237.3:c.587G= MANE Select NP_079513.1:p.Arg196=
Search 100 bp 5'
Search 100 bp 3'