Canonical Allele Identifier: CA13336108
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs915906

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133530234C>T , CM000672.2:g.133530234C>T GRCh38
NC_000010.10:g.135343738C>T , CM000672.1:g.135343738C>T GRCh37
NC_000010.9:g.135193728C>T NCBI36
NG_008383.1:g.7872C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.338-1351C>T MANE Select ENSP00000252945.3:n.338-1351C>T
ENST00000252945.7:c.338-1351C>T ENSP00000252945.3:n.338-1351C>T
ENST00000418356.1:n.77-1890C>T ENSP00000397299.1:n.77-1890C>T
ENST00000421586.5:n.77-1351C>T ENSP00000412754.1:n.77-1351C>T
ENST00000463117.6:c.338-1351C>T ENSP00000440689.1:n.338-1351C>T
ENST00000477500.5:n.299-1351C>T
ENST00000480558.1:n.563-1351C>T
ENST00000541080.5:n.77-1351C>T
NM_000773.3:c.338-1351C>T NP_000764.1:n.338-1351C>T
NM_000773.4:c.338-1351C>T MANE Select NP_000764.1:n.338-1351C>T