Canonical Allele Identifier: CA1946816342
Gene: CYP2E1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538605C= , CM000672.2:g.133538605C= GRCh38
NC_000010.10:g.135352109C= , CM000672.1:g.135352109C= GRCh37
NC_000010.9:g.135202099C= NCBI36
NG_008383.1:g.16243C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.1298-175C= MANE Select ENSP00000252945.3:n.1298-175C=
ENST00000252945.7:c.1298-175C= ENSP00000252945.3:n.1298-175C=
ENST00000368520.1:n.1358+713C=
ENST00000418356.1:c.887-175C= ENSP00000397299.1:n.887-175C=
ENST00000421586.5:c.1037-175C= ENSP00000412754.1:n.1037-175C=
ENST00000463117.6:c.1298-175C= ENSP00000440689.1:n.1298-175C=
ENST00000469258.1:n.394-175C=
ENST00000541080.5:c.714-175C=
NM_000773.3:c.1298-175C= NP_000764.1:n.1298-175C=
NM_000773.4:c.1298-175C= MANE Select NP_000764.1:n.1298-175C=
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