Canonical Allele Identifier: CA1462694306
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558284C= , CM000666.2:g.62558284C= GRCh38
NC_000004.11:g.63424002C= , CM000666.1:g.63424002C= GRCh37
NC_000004.10:g.63106597C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5560C=