Canonical Allele Identifier: CA1946816563
Gene: CYP2E1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538733T= , CM000672.2:g.133538733T= GRCh38
NC_000010.10:g.135352237T= , CM000672.1:g.135352237T= GRCh37
NC_000010.9:g.135202227T= NCBI36
NG_008383.1:g.16371T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1298-47T= MANE Select ENSP00000252945.3:n.1298-47T=
ENST00000252945.7:c.1298-47T= ENSP00000252945.3:n.1298-47T=
ENST00000368520.1:n.1358+841T=
ENST00000418356.1:c.887-47T= ENSP00000397299.1:n.887-47T=
ENST00000421586.5:c.1037-47T= ENSP00000412754.1:n.1037-47T=
ENST00000463117.6:c.1298-47T= ENSP00000440689.1:n.1298-47T=
ENST00000469258.1:n.394-47T=
ENST00000541080.5:c.714-47T=
NM_000773.3:c.1298-47T= NP_000764.1:n.1298-47T=
NM_000773.4:c.1298-47T= MANE Select NP_000764.1:n.1298-47T=
Search 100 bp 5'
Search 100 bp 3'