Canonical Allele Identifier: CA596749351
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1333045454
gnomAD v2: 10-135352698-T-TTTTTTG
gnomAD v3: 10-133539194-T-TTTTTTG
gnomAD v4: 10-133539194-T-TTTTTTG
MyVariant Identifiers: chr10:g.135352698_135352699insTTTTTG (hg19) chr10:g.133539194_133539195insTTTTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539199_133539200insGTTTTT , CM000672.2:g.133539199_133539200insGTTTTT GRCh38
NC_000010.10:g.135352703_135352704insGTTTTT , CM000672.1:g.135352703_135352704insGTTTTT GRCh37
NC_000010.9:g.135202693_135202694insGTTTTT NCBI36
NG_008383.1:g.16837_16838insGTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1307_1358+1308insGTTTTT
Search 100 bp 5'
Search 100 bp 3'