Canonical Allele Identifier: CA587286152

Gene:

Linked Data

• dbSNP Id: rs886371119
• gnomAD v2: 9-25551233-T-A
• MyVariant Identifiers: chr9:g.25551233T>A (hg19) ; chr9:g.25551235T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551235T>A , CM000671.2:g.25551235T>A	GRCh38
NC_000009.11:g.25551233T>A , CM000671.1:g.25551233T>A	GRCh37
NC_000009.10:g.25541233T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-663A>T
XR_929525.2:n.674-663A>T