Canonical Allele Identifier: CA2761911330
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558207C>T , CM000666.2:g.62558207C>T GRCh38
NC_000004.11:g.63423925C>T , CM000666.1:g.63423925C>T GRCh37
NC_000004.10:g.63106520C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5637C>T