Canonical Allele Identifier: CA1462694385
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558466T= , CM000666.2:g.62558466T= GRCh38
NC_000004.11:g.63424184T= , CM000666.1:g.63424184T= GRCh37
NC_000004.10:g.63106779T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5378T=