Canonical Allele Identifier: CA862568137

Gene:

Linked Data

• dbSNP Id: rs1459798458
• MyVariant Identifiers: chr9:g.25551347T>A (hg19) ; chr9:g.25551349T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551349T>A , CM000671.2:g.25551349T>A	GRCh38
NC_000009.11:g.25551347T>A , CM000671.1:g.25551347T>A	GRCh37
NC_000009.10:g.25541347T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-777A>T
XR_929525.2:n.674-777A>T