Canonical Allele Identifier: CA785288247
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs1379984991

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460454C>T , CM000666.2:g.110460454C>T GRCh38
NC_000004.11:g.111381610C>T , CM000666.1:g.111381610C>T GRCh37
NC_000004.10:g.111601059C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28087C>T