Canonical Allele Identifier: CA1912720832
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812745A= , CM000672.2:g.57812745A= GRCh38
NC_000010.10:g.59572505A= , CM000672.1:g.59572505A= GRCh37
NC_000010.9:g.59242511A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34547T=
XR_001747454.1:n.85+34547T=