Canonical Allele Identifier: CA216857796

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1022723490
• gnomAD v3: 10-133531990-T-C
• gnomAD v4: 10-133531990-T-C
• MyVariant Identifiers: chr10:g.135345494T>C (hg19) ; chr10:g.133531990T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133531990T>C , CM000672.2:g.133531990T>C	GRCh38
NC_000010.10:g.135345494T>C , CM000672.1:g.135345494T>C	GRCh37
NC_000010.9:g.135195484T>C	NCBI36
NG_008383.1:g.9628T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252945.8:c.488-134T>C MANE Select	ENSP00000252945.3:n.488-134T>C
ENST00000252945.7:c.488-134T>C	ENSP00000252945.3:n.488-134T>C
ENST00000368520.1:n.415T>C
ENST00000418356.1:c.77-134T>C	ENSP00000397299.1:n.77-134T>C
ENST00000421586.5:c.227-134T>C	ENSP00000412754.1:n.227-134T>C
ENST00000463117.6:c.488-134T>C	ENSP00000440689.1:n.488-134T>C
ENST00000477500.5:n.448+256T>C
ENST00000480558.1:n.713-134T>C
ENST00000541080.5:c.226+256T>C
NM_000773.3:c.488-134T>C	NP_000764.1:n.488-134T>C
NM_000773.4:c.488-134T>C MANE Select	NP_000764.1:n.488-134T>C