Canonical Allele Identifier: CA2611616974
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133539109-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539111dup , CM000672.2:g.133539111dup GRCh38
NC_000010.10:g.135352615dup , CM000672.1:g.135352615dup GRCh37
NC_000010.9:g.135202605dup NCBI36
NG_008383.1:g.16749dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*147dup MANE Select ENSP00000252945.3:n.*147dup
ENST00000252945.7:c.*147dup ENSP00000252945.3:n.*147dup
ENST00000368520.1:n.1358+1219dup
ENST00000463117.6:c.*147dup ENSP00000440689.1:n.*147dup
ENST00000469258.1:n.725dup
NM_000773.3:c.*147dup NP_000764.1:n.*147dup
NM_000773.4:c.*147dup MANE Select NP_000764.1:n.*147dup
Search 100 bp 5'
Search 100 bp 3'