Canonical Allele Identifier: CA253291
Gene: SOST HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4785
ClinVar RCV Id: RCV000005051
dbSNP Id: rs104894644

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755612C>T , CM000679.2:g.43755612C>T GRCh38
NC_000017.9:g.39188506C>T NCBI36
NC_000017.10:g.41832980C>T , CM000679.1:g.41832980C>T GRCh37
NG_008078.2:g.8177G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301691.2:c.372G>A ENSP00000301691.1:p.Trp124Ter
NM_025237.2:c.372G>A VV NP_079513.1:p.Trp124Ter