Canonical Allele Identifier: CA2581300322
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376331C>A , CM000679.2:g.29376331C>A GRCh38
NC_000017.10:g.27703349C>A , CM000679.1:g.27703349C>A GRCh37
NC_000017.9:g.24727475C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-6026G>T XP_011523890.1:n.1008-6026G>T