Canonical Allele Identifier: CA2013540849
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5284178T= , CM000674.2:g.5284178T= GRCh38
NC_000012.11:g.5393344T= , CM000674.1:g.5393344T= GRCh37
NC_000012.10:g.5263605T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931576.1:n.611+7289T=
XR_931577.1:n.611+7289T=
XR_001748970.1:n.594+7289T=