Canonical Allele Identifier: CA2788132301
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812992G>A , CM000672.2:g.57812992G>A GRCh38
NC_000010.10:g.59572752G>A , CM000672.1:g.59572752G>A GRCh37
NC_000010.9:g.59242758G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34300C>T
XR_001747454.1:n.85+34300C>T