Canonical Allele Identifier: CA2254736389
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376365G= , CM000679.2:g.29376365G= GRCh38
NC_000017.10:g.27703383G= , CM000679.1:g.27703383G= GRCh37
NC_000017.9:g.24727509G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-6060C= XP_011523890.1:n.1008-6060C=