Canonical Allele Identifier: CA2580598451
Gene:

Genomic Alleles

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

Transcript Alleles

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