Canonical Allele Identifier: CA1462694386
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558467T= , CM000666.2:g.62558467T= GRCh38
NC_000004.11:g.63424185T= , CM000666.1:g.63424185T= GRCh37
NC_000004.10:g.63106780T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5377T=