Canonical Allele Identifier: CA500234877
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41832785C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755417C>T , CM000679.2:g.43755417C>T GRCh38
NC_000017.10:g.41832785C>T , CM000679.1:g.41832785C>T GRCh37
NC_000017.9:g.39188311C>T NCBI36
NG_008078.2:g.8372G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301691.3:c.567G>A MANE Select ENSP00000301691.1:p.Pro189=
ENST00000301691.2:c.567G>A ENSP00000301691.1:p.Pro189=
NM_025237.2:c.567G>A NP_079513.1:p.Pro189=
NM_025237.3:c.567G>A MANE Select NP_079513.1:p.Pro189=