Canonical Allele Identifier: CA2781411969
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269778G>A , CM000670.2:g.97269778G>A GRCh38
NC_000008.10:g.98282006G>A , CM000670.1:g.98282006G>A GRCh37
NC_000008.9:g.98351182G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149292C>T