Canonical Allele Identifier: CA862568134

Gene:

Linked Data

• dbSNP Id: rs1296743579
• MyVariant Identifiers: chr9:g.25551346T>G (hg19) ; chr9:g.25551348T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551348T>G , CM000671.2:g.25551348T>G	GRCh38
NC_000009.11:g.25551346T>G , CM000671.1:g.25551346T>G	GRCh37
NC_000009.10:g.25541346T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-776A>C
XR_929525.2:n.674-776A>C