Canonical Allele Identifier: CA2761911328
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558156T>G , CM000666.2:g.62558156T>G GRCh38
NC_000004.11:g.63423874T>G , CM000666.1:g.63423874T>G GRCh37
NC_000004.10:g.63106469T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5688T>G