Canonical Allele Identifier: CA2517494575
Gene: ENPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460425T>A , CM000666.2:g.110460425T>A GRCh38
NC_000004.11:g.111381581T>A , CM000666.1:g.111381581T>A GRCh37
NC_000004.10:g.111601030T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28116T>A