Canonical Allele Identifier: CA216859264
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs972825608
gnomAD v3: 10-133539229-A-C
gnomAD v4: 10-133539229-A-C
MyVariant Identifiers: chr10:g.135352733A>C (hg19) chr10:g.133539229A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539229A>C , CM000672.2:g.133539229A>C GRCh38
NC_000010.10:g.135352733A>C , CM000672.1:g.135352733A>C GRCh37
NC_000010.9:g.135202723A>C NCBI36
NG_008383.1:g.16867A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1337A>C
Search 100 bp 5'
Search 100 bp 3'