Canonical Allele Identifier: CA1462694182
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558052T= , CM000666.2:g.62558052T= GRCh38
NC_000004.11:g.63423770T= , CM000666.1:g.63423770T= GRCh37
NC_000004.10:g.63106365T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5792T=