Canonical Allele Identifier: CA1912720960
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812995A= , CM000672.2:g.57812995A= GRCh38
NC_000010.10:g.59572755A= , CM000672.1:g.59572755A= GRCh37
NC_000010.9:g.59242761A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34297T=
XR_001747454.1:n.85+34297T=