Canonical Allele Identifier: CA103713966

Gene: ENPEP

Linked Data

• dbSNP Id: rs544076632
• gnomAD v3: 4-110460531-G-A
• gnomAD v4: 4-110460531-G-A
• MyVariant Identifiers: chr4:g.111381687G>A (hg19) ; chr4:g.110460531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110460531G>A , CM000666.2:g.110460531G>A	GRCh38
NC_000004.11:g.111381687G>A , CM000666.1:g.111381687G>A	GRCh37
NC_000004.10:g.111601136G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510961.1:n.73-28010G>A