Canonical Allele Identifier: CA2568618742
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269666G>A , CM000670.2:g.97269666G>A GRCh38
NC_000008.10:g.98281894G>A , CM000670.1:g.98281894G>A GRCh37
NC_000008.9:g.98351070G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149404C>T