Canonical Allele Identifier: CA2246165746
Gene:

Linked Data

dbSNP Id: rs1981890139

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137378G>A , CM000679.2:g.8137378G>A GRCh38
NC_000017.10:g.8040696G>A , CM000679.1:g.8040696G>A GRCh37
NC_000017.9:g.7981421G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1471G>A
XR_934203.1:n.70-2099G>A
XR_934202.2:n.414-1471G>A