Canonical Allele Identifier: CA378835270

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1851346822
• gnomAD v3: 10-133532181-A-G
• gnomAD v4: 10-133532181-A-G
• MyVariant Identifiers: chr10:g.135345685A>G (hg19) ; chr10:g.133532181A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133532181A>G , CM000672.2:g.133532181A>G	GRCh38
NC_000010.10:g.135345685A>G , CM000672.1:g.135345685A>G	GRCh37
NC_000010.9:g.135195675A>G	NCBI36
NG_008383.1:g.9819A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.545A>G MANE Select	ENSP00000252945.3:p.Asp182Gly
ENST00000252945.7:c.545A>G	ENSP00000252945.3:p.Asp182Gly
ENST00000368520.1:n.606A>G
ENST00000418356.1:c.134A>G	ENSP00000397299.1:p.Asp45Gly
ENST00000421586.5:c.284A>G	ENSP00000412754.1:p.Asp95Gly
ENST00000463117.6:c.545A>G	ENSP00000440689.1:p.Asp182Gly
ENST00000477500.5:n.448+447A>G
ENST00000541080.5:c.226+447A>G
NM_000773.3:c.545A>G	NP_000764.1:p.Asp182Gly
NM_000773.4:c.545A>G MANE Select	NP_000764.1:p.Asp182Gly