Canonical Allele Identifier: CA2549687900
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84170229C>T , CM000674.2:g.84170229C>T GRCh38
NC_000012.11:g.84564008C>T , CM000674.1:g.84564008C>T GRCh37
NC_000012.10:g.83088139C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749234.1:n.127+16237G>A
XR_001749235.1:n.127+16237G>A