Canonical Allele Identifier: CA596749352
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v2: 10-135352700-T-TG
MyVariant Identifiers: chr10:g.135352700_135352701insG (hg19) chr10:g.133539196_133539197insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539196_133539197insG , CM000672.2:g.133539196_133539197insG GRCh38
NC_000010.10:g.135352700_135352701insG , CM000672.1:g.135352700_135352701insG GRCh37
NC_000010.9:g.135202690_135202691insG NCBI36
NG_008383.1:g.16834_16835insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1304_1358+1305insG
Search 100 bp 5'
Search 100 bp 3'