Canonical Allele Identifier: CA500234875
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755417-C-A
MyVariant Identifiers: chr17:g.41832785C>A (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000301691.3:c.567G>T MANE Select ENSP00000301691.1:p.Pro189=
ENST00000301691.2:c.567G>T ENSP00000301691.1:p.Pro189=
NM_025237.2:c.567G>T NP_079513.1:p.Pro189=
NM_025237.3:c.567G>T MANE Select NP_079513.1:p.Pro189=
Search 100 bp 5'
Search 100 bp 3'