Canonical Allele Identifier: CA378842686
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1589957815

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538905C>T , CM000672.2:g.133538905C>T GRCh38
NC_000010.10:g.135352409C>T , CM000672.1:g.135352409C>T GRCh37
NC_000010.9:g.135202399C>T NCBI36
NG_008383.1:g.16543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1423C>T MANE Select ENSP00000252945.3:p.His475Tyr
ENST00000252945.7:c.1423C>T ENSP00000252945.3:p.His475Tyr
ENST00000368520.1:n.1358+1013C>T
ENST00000463117.6:c.1423C>T ENSP00000440689.1:p.His475Tyr
ENST00000469258.1:n.519C>T
NM_000773.3:c.1423C>T NP_000764.1:p.His475Tyr
NM_000773.4:c.1423C>T MANE Select NP_000764.1:p.His475Tyr