Canonical Allele Identifier: CA472244229

Gene: CYP2E1

Linked Data

• MyVariant Identifiers: chr10:g.135345506C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532002C>G , CM000672.2:g.133532002C>G	GRCh38
NC_000010.10:g.135345506C>G , CM000672.1:g.135345506C>G	GRCh37
NC_000010.9:g.135195496C>G	NCBI36
NG_008383.1:g.9640C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.488-122C>G MANE Select	ENSP00000252945.3:n.488-122C>G
ENST00000252945.7:c.488-122C>G	ENSP00000252945.3:n.488-122C>G
ENST00000368520.1:n.427C>G
ENST00000418356.1:c.77-122C>G	ENSP00000397299.1:n.77-122C>G
ENST00000421586.5:c.227-122C>G	ENSP00000412754.1:n.227-122C>G
ENST00000463117.6:c.488-122C>G	ENSP00000440689.1:n.488-122C>G
ENST00000477500.5:n.448+268C>G
ENST00000480558.1:n.713-122C>G
ENST00000541080.5:c.226+268C>G
NM_000773.3:c.488-122C>G	NP_000764.1:n.488-122C>G
NM_000773.4:c.488-122C>G MANE Select	NP_000764.1:n.488-122C>G