Canonical Allele Identifier: CA399702122
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1974121166

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755640A>G , CM000679.2:g.43755640A>G GRCh38
NC_000017.10:g.41833008A>G , CM000679.1:g.41833008A>G GRCh37
NC_000017.9:g.39188534A>G NCBI36
NG_008078.2:g.8149T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.344T>C MANE Select ENSP00000301691.1:p.Leu115Pro
ENST00000301691.2:c.344T>C ENSP00000301691.1:p.Leu115Pro
NM_025237.2:c.344T>C NP_079513.1:p.Leu115Pro
NM_025237.3:c.344T>C MANE Select NP_079513.1:p.Leu115Pro