Canonical Allele Identifier: CA1462694304
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558282T= , CM000666.2:g.62558282T= GRCh38
NC_000004.11:g.63424000T= , CM000666.1:g.63424000T= GRCh37
NC_000004.10:g.63106595T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5562T=