Canonical Allele Identifier: CA2763070656
Gene: ENPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460417A>C , CM000666.2:g.110460417A>C GRCh38
NC_000004.11:g.111381573A>C , CM000666.1:g.111381573A>C GRCh37
NC_000004.10:g.111601022A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28124A>C