Canonical Allele Identifier: CA2535649921
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529668C>T , CM000674.2:g.131529668C>T GRCh38
NC_000012.11:g.132014213C>T , CM000674.1:g.132014213C>T GRCh37
NC_000012.10:g.130580166C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+107G>A
XR_001749407.2:n.1067+107G>A