Canonical Allele Identifier: CA103713948

Gene: ENPEP

Linked Data

• dbSNP Id: rs766898537
• gnomAD v2: 4-111381644-T-C
• gnomAD v3: 4-110460488-T-C
• gnomAD v4: 4-110460488-T-C
• MyVariant Identifiers: chr4:g.111381644T>C (hg19) ; chr4:g.110460488T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110460488T>C , CM000666.2:g.110460488T>C	GRCh38
NC_000004.11:g.111381644T>C , CM000666.1:g.111381644T>C	GRCh37
NC_000004.10:g.111601093T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510961.1:n.73-28053T>C