Canonical Allele Identifier: CA2580598452
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366755A>T , CM000672.2:g.3366755A>T GRCh38
NC_000010.10:g.3408947A>T , CM000672.1:g.3408947A>T GRCh37
NC_000010.9:g.3398947A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47899A>T