Canonical Allele Identifier: CA2761911331
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558211C>A , CM000666.2:g.62558211C>A GRCh38
NC_000004.11:g.63423929C>A , CM000666.1:g.63423929C>A GRCh37
NC_000004.10:g.63106524C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5633C>A