Canonical Allele Identifier: CA662011964
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1482581657
gnomAD v3: 10-133539137-AAT-A
gnomAD v4: 10-133539137-AAT-A
MyVariant Identifiers: chr10:g.135352642_135352643del (hg19) chr10:g.133539138_133539139del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539140_133539141del , CM000672.2:g.133539140_133539141del GRCh38
NC_000010.10:g.135352644_135352645del , CM000672.1:g.135352644_135352645del GRCh37
NC_000010.9:g.135202634_135202635del NCBI36
NG_008383.1:g.16778_16779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1248_1358+1249del
Search 100 bp 5'
Search 100 bp 3'