Canonical Allele Identifier: CA662022599
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1296430810
gnomAD v3: 10-133526811-G-A
gnomAD v4: 10-133526811-G-A
MyVariant Identifiers: chr10:g.135340315G>A (hg19) chr10:g.133526811G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526811G>A , CM000672.2:g.133526811G>A GRCh38
NC_000010.10:g.135340315G>A , CM000672.1:g.135340315G>A GRCh37
NC_000010.9:g.135190305G>A NCBI36
NG_008383.1:g.4449G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-102G>A ENSP00000440689.1:n.-102G>A
ENST00000541261.1:c.-102G>A ENSP00000437799.1:n.-102G>A
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