Canonical Allele Identifier: CA103713935
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs1034403593

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460467A>G , CM000666.2:g.110460467A>G GRCh38
NC_000004.11:g.111381623A>G , CM000666.1:g.111381623A>G GRCh37
NC_000004.10:g.111601072A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28074A>G