Canonical Allele Identifier: CA662011466

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1162550504
• MyVariant Identifiers: chr10:g.135352079G>C (hg19) ; chr10:g.133538575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538575G>C , CM000672.2:g.133538575G>C	GRCh38
NC_000010.10:g.135352079G>C , CM000672.1:g.135352079G>C	GRCh37
NC_000010.9:g.135202069G>C	NCBI36
NG_008383.1:g.16213G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.1298-205G>C MANE Select	ENSP00000252945.3:n.1298-205G>C
ENST00000252945.7:c.1298-205G>C	ENSP00000252945.3:n.1298-205G>C
ENST00000368520.1:n.1358+683G>C
ENST00000418356.1:c.887-205G>C	ENSP00000397299.1:n.887-205G>C
ENST00000421586.5:c.1037-205G>C	ENSP00000412754.1:n.1037-205G>C
ENST00000463117.6:c.1298-205G>C	ENSP00000440689.1:n.1298-205G>C
ENST00000469258.1:n.394-205G>C
ENST00000541080.5:c.714-205G>C
NM_000773.3:c.1298-205G>C	NP_000764.1:n.1298-205G>C
NM_000773.4:c.1298-205G>C MANE Select	NP_000764.1:n.1298-205G>C