Canonical Allele Identifier: CA2254736392
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376371T= , CM000679.2:g.29376371T= GRCh38
NC_000017.10:g.27703389T= , CM000679.1:g.27703389T= GRCh37
NC_000017.9:g.24727515T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-6066A= XP_011523890.1:n.1008-6066A=