Canonical Allele Identifier: CA216859263
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs7092804
gnomAD v2: 10-135352721-T-C
gnomAD v3: 10-133539217-T-C
gnomAD v4: 10-133539217-T-C
MyVariant Identifiers: chr10:g.135352721T>C (hg19) chr10:g.133539217T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539217T>C , CM000672.2:g.133539217T>C GRCh38
NC_000010.10:g.135352721T>C , CM000672.1:g.135352721T>C GRCh37
NC_000010.9:g.135202711T>C NCBI36
NG_008383.1:g.16855T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1325T>C
Search 100 bp 5'
Search 100 bp 3'