Canonical Allele Identifier: CA2024044979
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.27812217C>A , CM000674.2:g.27812217C>A GRCh38
NC_000012.11:g.27965150C>A , CM000674.1:g.27965150C>A GRCh37
NC_000012.10:g.27856417C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931459.1:n.237-816G>T
XR_001749449.1:n.197-816G>T
XR_931459.2:n.222-816G>T