Canonical Allele Identifier: CA2536111435
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376408A>G , CM000679.2:g.29376408A>G GRCh38
NC_000017.10:g.27703426A>G , CM000679.1:g.27703426A>G GRCh37
NC_000017.9:g.24727552A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-6103T>C XP_011523890.1:n.1008-6103T>C