Canonical Allele Identifier: CA1485062913
Gene: ENPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460531G= , CM000666.2:g.110460531G= GRCh38
NC_000004.11:g.111381687G= , CM000666.1:g.111381687G= GRCh37
NC_000004.10:g.111601136G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28010G=