Canonical Allele Identifier: CA103713929
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs570029584

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460432G>A , CM000666.2:g.110460432G>A GRCh38
NC_000004.11:g.111381588G>A , CM000666.1:g.111381588G>A GRCh37
NC_000004.10:g.111601037G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28109G>A