Canonical Allele Identifier: CA1946816815
Gene: CYP2E1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538852A= , CM000672.2:g.133538852A= GRCh38
NC_000010.10:g.135352356A= , CM000672.1:g.135352356A= GRCh37
NC_000010.9:g.135202346A= NCBI36
NG_008383.1:g.16490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1370A= MANE Select ENSP00000252945.3:p.His457=
ENST00000252945.7:c.1370A= ENSP00000252945.3:p.His457=
ENST00000368520.1:n.1358+960A=
ENST00000463117.6:c.1370A= ENSP00000440689.1:p.His457=
ENST00000469258.1:n.466A=
NM_000773.3:c.1370A= NP_000764.1:p.His457=
NM_000773.4:c.1370A= MANE Select NP_000764.1:p.His457=
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