Canonical Allele Identifier: CA858377712

Gene:

Linked Data

• dbSNP Id: rs1192537829
• MyVariant Identifiers: chr9:g.110855327G>A (hg19) ; chr9:g.108093046G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108093046G>A , CM000671.2:g.108093046G>A	GRCh38
NC_000009.11:g.110855327G>A , CM000671.1:g.110855327G>A	GRCh37
NC_000009.10:g.109895148G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930239.1:n.461-39752C>T
XR_001746881.1:n.668-39752C>T
XR_001746882.1:n.668-39752C>T