Canonical Allele Identifier: CA378842121
Gene: CYP2E1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.135352311T>C (hg19) chr10:g.133538807T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538807T>C , CM000672.2:g.133538807T>C GRCh38
NC_000010.10:g.135352311T>C , CM000672.1:g.135352311T>C GRCh37
NC_000010.9:g.135202301T>C NCBI36
NG_008383.1:g.16445T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1325T>C MANE Select ENSP00000252945.3:p.Leu442Pro
ENST00000252945.7:c.1325T>C ENSP00000252945.3:p.Leu442Pro
ENST00000368520.1:n.1358+915T>C
ENST00000418356.1:c.914T>C ENSP00000397299.1:p.Leu305Pro
ENST00000421586.5:c.1064T>C ENSP00000412754.1:p.Leu355Pro
ENST00000463117.6:c.1325T>C ENSP00000440689.1:p.Leu442Pro
ENST00000469258.1:n.421T>C
ENST00000541080.5:c.741T>C
NM_000773.3:c.1325T>C NP_000764.1:p.Leu442Pro
NM_000773.4:c.1325T>C MANE Select NP_000764.1:p.Leu442Pro
Search 100 bp 5'
Search 100 bp 3'