Canonical Allele Identifier: CA662012280
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1236686299
gnomAD v2: 10-135352728-C-T
gnomAD v3: 10-133539224-C-T
gnomAD v4: 10-133539224-C-T
MyVariant Identifiers: chr10:g.135352728C>T (hg19) chr10:g.133539224C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539224C>T , CM000672.2:g.133539224C>T GRCh38
NC_000010.10:g.135352728C>T , CM000672.1:g.135352728C>T GRCh37
NC_000010.9:g.135202718C>T NCBI36
NG_008383.1:g.16862C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1332C>T
Search 100 bp 5'
Search 100 bp 3'