Canonical Allele Identifier: CA8592807
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs775244532

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755646C>T , CM000679.2:g.43755646C>T GRCh38
NC_000017.10:g.41833014C>T , CM000679.1:g.41833014C>T GRCh37
NC_000017.9:g.39188540C>T NCBI36
NG_008078.2:g.8143G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.338G>A MANE Select ENSP00000301691.1:p.Arg113His
ENST00000301691.2:c.338G>A ENSP00000301691.1:p.Arg113His
NM_025237.2:c.338G>A NP_079513.1:p.Arg113His
NM_025237.3:c.338G>A MANE Select NP_079513.1:p.Arg113His