Canonical Allele Identifier: CA472261793

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1851438375
• MyVariant Identifiers: chr10:g.135352291A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538787A>C , CM000672.2:g.133538787A>C	GRCh38
NC_000010.10:g.135352291A>C , CM000672.1:g.135352291A>C	GRCh37
NC_000010.9:g.135202281A>C	NCBI36
NG_008383.1:g.16425A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1305A>C MANE Select	ENSP00000252945.3:p.Arg435=
ENST00000252945.7:c.1305A>C	ENSP00000252945.3:p.Arg435=
ENST00000368520.1:n.1358+895A>C
ENST00000418356.1:c.894A>C	ENSP00000397299.1:p.Arg298=
ENST00000421586.5:c.1044A>C	ENSP00000412754.1:p.Arg348=
ENST00000463117.6:c.1305A>C	ENSP00000440689.1:p.Arg435=
ENST00000469258.1:n.401A>C
ENST00000541080.5:c.721A>C
NM_000773.3:c.1305A>C	NP_000764.1:p.Arg435=
NM_000773.4:c.1305A>C MANE Select	NP_000764.1:p.Arg435=