Canonical Allele Identifier: CA2611617196
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539198-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539198T>A , CM000672.2:g.133539198T>A GRCh38
NC_000010.10:g.135352702T>A , CM000672.1:g.135352702T>A GRCh37
NC_000010.9:g.135202692T>A NCBI36
NG_008383.1:g.16836T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1306T>A
Search 100 bp 5'
Search 100 bp 3'