Canonical Allele Identifier: CA2706730527
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs2110320664

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460485A>G , CM000666.2:g.110460485A>G GRCh38
NC_000004.11:g.111381641A>G , CM000666.1:g.111381641A>G GRCh37
NC_000004.10:g.111601090A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28056A>G