Canonical Allele Identifier: CA2809140969
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376346T>A , CM000679.2:g.29376346T>A GRCh38
NC_000017.10:g.27703364T>A , CM000679.1:g.27703364T>A GRCh37
NC_000017.9:g.24727490T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011525588.1:c.1008-6041A>T XP_011523890.1:n.1008-6041A>T