Canonical Allele Identifier: CA2261069244
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755632C= , CM000679.2:g.43755632C= GRCh38
NC_000017.10:g.41833000C= , CM000679.1:g.41833000C= GRCh37
NC_000017.9:g.39188526C= NCBI36
NG_008078.2:g.8157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.352G= MANE Select ENSP00000301691.1:p.Ala118=
ENST00000301691.2:c.352G= ENSP00000301691.1:p.Ala118=
NM_025237.2:c.352G= NP_079513.1:p.Ala118=
NM_025237.3:c.352G= MANE Select NP_079513.1:p.Ala118=