Canonical Allele Identifier: CA596749400
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1436641204
gnomAD v2: 10-135352719-T-A
gnomAD v3: 10-133539215-T-A
gnomAD v4: 10-133539215-T-A
MyVariant Identifiers: chr10:g.135352719T>A (hg19) chr10:g.133539215T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539215T>A , CM000672.2:g.133539215T>A GRCh38
NC_000010.10:g.135352719T>A , CM000672.1:g.135352719T>A GRCh37
NC_000010.9:g.135202709T>A NCBI36
NG_008383.1:g.16853T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1323T>A
Search 100 bp 5'
Search 100 bp 3'