Canonical Allele Identifier: CA1485062833
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs1723763703

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460390G>A , CM000666.2:g.110460390G>A GRCh38
NC_000004.11:g.111381546G>A , CM000666.1:g.111381546G>A GRCh37
NC_000004.10:g.111600995G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28151G>A