Canonical Allele Identifier: CA1462694311
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558296G= , CM000666.2:g.62558296G= GRCh38
NC_000004.11:g.63424014G= , CM000666.1:g.63424014G= GRCh37
NC_000004.10:g.63106609G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5548G=