Canonical Allele Identifier: CA216858358
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs4646976

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133534223A>G , CM000672.2:g.133534223A>G GRCh38
NC_000010.10:g.135347727A>G , CM000672.1:g.135347727A>G GRCh37
NC_000010.9:g.135197717A>G NCBI36
NG_008383.1:g.11861A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.967+326A>G MANE Select ENSP00000252945.3:n.967+326A>G
ENST00000252945.7:c.967+326A>G ENSP00000252945.3:n.967+326A>G
ENST00000368520.1:n.1028+326A>G
ENST00000418356.1:c.556+326A>G ENSP00000397299.1:n.556+326A>G
ENST00000421586.5:c.706+326A>G ENSP00000412754.1:n.706+326A>G
ENST00000463117.6:c.967+326A>G ENSP00000440689.1:n.967+326A>G
ENST00000541080.5:c.383+1355A>G
NM_000773.3:c.967+326A>G NP_000764.1:n.967+326A>G
NM_000773.4:c.967+326A>G MANE Select NP_000764.1:n.967+326A>G