Canonical Allele Identifier: CA103713960

Gene: ENPEP

Linked Data

• dbSNP Id: rs576588441
• gnomAD v3: 4-110460525-A-T
• gnomAD v4: 4-110460525-A-T
• MyVariant Identifiers: chr4:g.111381681A>T (hg19) ; chr4:g.110460525A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110460525A>T , CM000666.2:g.110460525A>T	GRCh38
NC_000004.11:g.111381681A>T , CM000666.1:g.111381681A>T	GRCh37
NC_000004.10:g.111601130A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510961.1:n.73-28016A>T