Canonical Allele Identifier: CA8592836
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs751927402
ExAC: 17:41833181 C / T
gnomAD v4: 17-43755813-C-T
MyVariant Identifiers: chr17:g.41833181C>T (hg19) chr17:g.43755813C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755813C>T , CM000679.2:g.43755813C>T GRCh38
NC_000017.10:g.41833181C>T , CM000679.1:g.41833181C>T GRCh37
NC_000017.9:g.39188707C>T NCBI36
NG_008078.2:g.7976G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-50G>A MANE Select ENSP00000301691.1:n.221-50G>A
ENST00000301691.2:c.221-50G>A ENSP00000301691.1:n.221-50G>A
NM_025237.2:c.221-50G>A NP_079513.1:n.221-50G>A
NM_025237.3:c.221-50G>A MANE Select NP_079513.1:n.221-50G>A
Search 100 bp 5'
Search 100 bp 3'