ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA785288260
Gene: ENPEP
HGNC
NCBI
Linked Data
dbSNP Id:
rs1283409654
MyVariant Identifiers:
chr4:g.111381655A>G (hg19)
chr4:g.110460499A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110460499A>G , CM000666.2:g.110460499A>G
GRCh38
NC_000004.11:g.111381655A>G , CM000666.1:g.111381655A>G
GRCh37
NC_000004.10:g.111601104A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000510961.1:n.73-28042A>G
Search 100 bp 5'
Search 100 bp 3'