Canonical Allele Identifier: CA191701695

Gene:

Linked Data

• dbSNP Id: rs1009085671
• MyVariant Identifiers: chr9:g.25551332T>C (hg19) ; chr9:g.25551334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551334T>C , CM000671.2:g.25551334T>C	GRCh38
NC_000009.11:g.25551332T>C , CM000671.1:g.25551332T>C	GRCh37
NC_000009.10:g.25541332T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-762A>G
XR_929525.2:n.674-762A>G