Canonical Allele Identifier: CA1485062839
Gene: ENPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460408G= , CM000666.2:g.110460408G= GRCh38
NC_000004.11:g.111381564G= , CM000666.1:g.111381564G= GRCh37
NC_000004.10:g.111601013G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28133G=