Canonical Allele Identifier: CA2520793580
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557942C>T , CM000666.2:g.62557942C>T GRCh38
NC_000004.11:g.63423660C>T , CM000666.1:g.63423660C>T GRCh37
NC_000004.10:g.63106255C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5902C>T