Canonical Allele Identifier: CA1462694253
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558173G= , CM000666.2:g.62558173G= GRCh38
NC_000004.11:g.63423891G= , CM000666.1:g.63423891G= GRCh37
NC_000004.10:g.63106486G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5671G=