Canonical Allele Identifier: CA2261069188
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755527C= , CM000679.2:g.43755527C= GRCh38
NC_000017.10:g.41832895C= , CM000679.1:g.41832895C= GRCh37
NC_000017.9:g.39188421C= NCBI36
NG_008078.2:g.8262G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.457G= MANE Select ENSP00000301691.1:p.Ala153=
ENST00000301691.2:c.457G= ENSP00000301691.1:p.Ala153=
NM_025237.2:c.457G= NP_079513.1:p.Ala153=
NM_025237.3:c.457G= MANE Select NP_079513.1:p.Ala153=