Canonical Allele Identifier: CA378842446
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133538857-A-G
MyVariant Identifiers: chr10:g.135352361A>G (hg19) chr10:g.133538857A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133538857A>G , CM000672.2:g.133538857A>G GRCh38
NC_000010.10:g.135352361A>G , CM000672.1:g.135352361A>G GRCh37
NC_000010.9:g.135202351A>G NCBI36
NG_008383.1:g.16495A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.1375A>G MANE Select ENSP00000252945.3:p.Asn459Asp
ENST00000252945.7:c.1375A>G ENSP00000252945.3:p.Asn459Asp
ENST00000368520.1:n.1358+965A>G
ENST00000463117.6:c.1375A>G ENSP00000440689.1:p.Asn459Asp
ENST00000469258.1:n.471A>G
NM_000773.3:c.1375A>G NP_000764.1:p.Asn459Asp
NM_000773.4:c.1375A>G MANE Select NP_000764.1:p.Asn459Asp
Search 100 bp 5'
Search 100 bp 3'