Canonical Allele Identifier: CA2548871096
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812832A>T , CM000672.2:g.57812832A>T GRCh38
NC_000010.10:g.59572592A>T , CM000672.1:g.59572592A>T GRCh37
NC_000010.9:g.59242598A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34460T>A
XR_001747454.1:n.85+34460T>A