Canonical Allele Identifier: CA1946830044
Gene: CYP2E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532105C= , CM000672.2:g.133532105C= GRCh38
NC_000010.10:g.135345609C= , CM000672.1:g.135345609C= GRCh37
NC_000010.9:g.135195599C= NCBI36
NG_008383.1:g.9743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.488-19C= MANE Select ENSP00000252945.3:n.488-19C=
ENST00000252945.7:c.488-19C= ENSP00000252945.3:n.488-19C=
ENST00000368520.1:n.530C=
ENST00000418356.1:c.77-19C= ENSP00000397299.1:n.77-19C=
ENST00000421586.5:c.227-19C= ENSP00000412754.1:n.227-19C=
ENST00000463117.6:c.488-19C= ENSP00000440689.1:n.488-19C=
ENST00000477500.5:n.448+371C=
ENST00000480558.1:n.713-19C=
ENST00000541080.5:c.226+371C=
NM_000773.3:c.488-19C= NP_000764.1:n.488-19C=
NM_000773.4:c.488-19C= MANE Select NP_000764.1:n.488-19C=