Canonical Allele Identifier: CA13420465
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68678956C>T , CM000673.2:g.68678956C>T GRCh38
NC_000011.9:g.68446424C>T , CM000673.1:g.68446424C>T GRCh37
NC_000011.8:g.68203000C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748281.1:n.231-1966G>A