Canonical Allele Identifier: CA626222057
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1368099332
gnomAD v2: 17-41833152-G-A
MyVariant Identifiers: chr17:g.41833152G>A (hg19) chr17:g.43755784G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755784G>A , CM000679.2:g.43755784G>A GRCh38
NC_000017.10:g.41833152G>A , CM000679.1:g.41833152G>A GRCh37
NC_000017.9:g.39188678G>A NCBI36
NG_008078.2:g.8005C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-21C>T MANE Select ENSP00000301691.1:n.221-21C>T
ENST00000301691.2:c.221-21C>T ENSP00000301691.1:n.221-21C>T
NM_025237.2:c.221-21C>T NP_079513.1:n.221-21C>T
NM_025237.3:c.221-21C>T MANE Select NP_079513.1:n.221-21C>T
Search 100 bp 5'
Search 100 bp 3'