Canonical Allele Identifier: CA191701692

Gene:

Linked Data

• dbSNP Id: rs904213007
• MyVariant Identifiers: chr9:g.25551296T>A (hg19) ; chr9:g.25551298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551298T>A , CM000671.2:g.25551298T>A	GRCh38
NC_000009.11:g.25551296T>A , CM000671.1:g.25551296T>A	GRCh37
NC_000009.10:g.25541296T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-726A>T
XR_929525.2:n.674-726A>T