Canonical Allele Identifier: CA596746468
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1487992604
gnomAD v2: 10-135340456-C-G
gnomAD v3: 10-133526952-C-G
gnomAD v4: 10-133526952-C-G
MyVariant Identifiers: chr10:g.135340456C>G (hg19) chr10:g.133526952C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526952C>G , CM000672.2:g.133526952C>G GRCh38
NC_000010.10:g.135340456C>G , CM000672.1:g.135340456C>G GRCh37
NC_000010.9:g.135190446C>G NCBI36
NG_008383.1:g.4590C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-40+79C>G ENSP00000440689.1:n.-40+79C>G
ENST00000541261.1:c.-40+79C>G ENSP00000437799.1:n.-40+79C>G
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