Canonical Allele Identifier: CA1485062905
Gene: ENPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460530A= , CM000666.2:g.110460530A= GRCh38
NC_000004.11:g.111381686A= , CM000666.1:g.111381686A= GRCh37
NC_000004.10:g.111601135A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28011A=