Canonical Allele Identifier: CA596749318
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1564850743
gnomAD v2: 10-135352681-T-TG
gnomAD v3: 10-133539177-T-TG
gnomAD v4: 10-133539177-T-TG
MyVariant Identifiers: chr10:g.135352681_135352682insG (hg19) chr10:g.133539177_133539178insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539177_133539178insG , CM000672.2:g.133539177_133539178insG GRCh38
NC_000010.10:g.135352681_135352682insG , CM000672.1:g.135352681_135352682insG GRCh37
NC_000010.9:g.135202671_135202672insG NCBI36
NG_008383.1:g.16815_16816insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1285_1358+1286insG
Search 100 bp 5'
Search 100 bp 3'