Canonical Allele Identifier: CA1946816975
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538911G= , CM000672.2:g.133538911G= GRCh38
NC_000010.10:g.135352415G= , CM000672.1:g.135352415G= GRCh37
NC_000010.9:g.135202405G= NCBI36
NG_008383.1:g.16549G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.1429G= MANE Select ENSP00000252945.3:p.Gly477=
ENST00000252945.7:c.1429G= ENSP00000252945.3:p.Gly477=
ENST00000368520.1:n.1358+1019G=
ENST00000463117.6:c.1429G= ENSP00000440689.1:p.Gly477=
ENST00000469258.1:n.525G=
NM_000773.3:c.1429G= NP_000764.1:p.Gly477=
NM_000773.4:c.1429G= MANE Select NP_000764.1:p.Gly477=