Canonical Allele Identifier: CA13337522

Gene: CYP2E1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133536297T>C , CM000672.2:g.133536297T>C	GRCh38
NC_000010.10:g.135349801T>C , CM000672.1:g.135349801T>C	GRCh37
NC_000010.9:g.135199791T>C	NCBI36
NG_008383.1:g.13935T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.968-766T>C MANE Select	ENSP00000252945.3:n.968-766T>C
ENST00000252945.7:c.968-766T>C	ENSP00000252945.3:n.968-766T>C
ENST00000368520.1:n.1029-766T>C
ENST00000418356.1:c.557-766T>C	ENSP00000397299.1:n.557-766T>C
ENST00000421586.5:c.707-766T>C	ENSP00000412754.1:n.707-766T>C
ENST00000463117.6:c.968-766T>C	ENSP00000440689.1:n.968-766T>C
ENST00000541080.5:c.384-766T>C
NM_000773.3:c.968-766T>C	NP_000764.1:n.968-766T>C
NM_000773.4:c.968-766T>C MANE Select	NP_000764.1:n.968-766T>C