Canonical Allele Identifier: CA2611613965
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133527187-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527187A>G , CM000672.2:g.133527187A>G GRCh38
NC_000010.10:g.135340691A>G , CM000672.1:g.135340691A>G GRCh37
NC_000010.9:g.135190681A>G NCBI36
NG_008383.1:g.4825A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-39-170A>G ENSP00000440689.1:n.-39-170A>G
ENST00000541261.1:c.-39-170A>G ENSP00000437799.1:n.-39-170A>G
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