Canonical Allele Identifier: CA1462694349
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558397T= , CM000666.2:g.62558397T= GRCh38
NC_000004.11:g.63424115T= , CM000666.1:g.63424115T= GRCh37
NC_000004.10:g.63106710T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5447T=