Canonical Allele Identifier: CA13911789
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.80143021G>A , CM000675.2:g.80143021G>A GRCh38
NC_000013.10:g.80717156G>A , CM000675.1:g.80717156G>A GRCh37
NC_000013.9:g.79615157G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942116.1:n.189-21145C>T
XR_942116.2:n.189-21145C>T