Canonical Allele Identifier: CA862568117

Gene:

Linked Data

• dbSNP Id: rs1223497052
• MyVariant Identifiers: chr9:g.25551303A>G (hg19) ; chr9:g.25551305A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551305A>G , CM000671.2:g.25551305A>G	GRCh38
NC_000009.11:g.25551303A>G , CM000671.1:g.25551303A>G	GRCh37
NC_000009.10:g.25541303A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-733T>C
XR_929525.2:n.674-733T>C