Canonical Allele Identifier: CA896967378

Gene:

Linked Data

• dbSNP Id: rs1165220183
• MyVariant Identifiers: chr3:g.109462385G>A (hg19) ; chr3:g.109743538G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743538G>A , CM000665.2:g.109743538G>A	GRCh38
NC_000003.11:g.109462385G>A , CM000665.1:g.109462385G>A	GRCh37
NC_000003.10:g.110945075G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63343G>A