Canonical Allele Identifier: CA2261069142
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755422G= , CM000679.2:g.43755422G= GRCh38
NC_000017.10:g.41832790G= , CM000679.1:g.41832790G= GRCh37
NC_000017.9:g.39188316G= NCBI36
NG_008078.2:g.8367C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.562C= MANE Select ENSP00000301691.1:p.Arg188=
ENST00000301691.2:c.562C= ENSP00000301691.1:p.Arg188=
NM_025237.2:c.562C= NP_079513.1:p.Arg188=
NM_025237.3:c.562C= MANE Select NP_079513.1:p.Arg188=