Canonical Allele Identifier: CA2289749546
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.22610832G>T , CM000680.2:g.22610832G>T GRCh38
NC_000018.9:g.20190795G>T , CM000680.1:g.20190795G>T GRCh37
NC_000018.8:g.18444793G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935284.1:n.88-639C>A
XR_935285.1:n.682-639C>A