Canonical Allele Identifier: CA1462694120
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557926A= , CM000666.2:g.62557926A= GRCh38
NC_000004.11:g.63423644A= , CM000666.1:g.63423644A= GRCh37
NC_000004.10:g.63106239A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5918A=