Canonical Allele Identifier: CA596749355
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851447449
gnomAD v2: 10-135352703-TTTTTGAGAG-T
gnomAD v3: 10-133539199-TTTTTGAGAG-T
gnomAD v4: 10-133539199-TTTTTGAGAG-T
MyVariant Identifiers: chr10:g.135352704_135352712del (hg19) chr10:g.133539200_133539208del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539205_133539213del , CM000672.2:g.133539205_133539213del GRCh38
NC_000010.10:g.135352709_135352717del , CM000672.1:g.135352709_135352717del GRCh37
NC_000010.9:g.135202699_135202707del NCBI36
NG_008383.1:g.16843_16851del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1313_1358+1321del
Search 100 bp 5'
Search 100 bp 3'