Canonical Allele Identifier: CA216859267
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs542594114
gnomAD v3: 10-133539251-T-G
gnomAD v4: 10-133539251-T-G
MyVariant Identifiers: chr10:g.135352755T>G (hg19) chr10:g.133539251T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539251T>G , CM000672.2:g.133539251T>G GRCh38
NC_000010.10:g.135352755T>G , CM000672.1:g.135352755T>G GRCh37
NC_000010.9:g.135202745T>G NCBI36
NG_008383.1:g.16889T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1359T>G
Search 100 bp 5'
Search 100 bp 3'