Canonical Allele Identifier: CA596749392
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851447790
gnomAD v2: 10-135352716-TGC-T
gnomAD v3: 10-133539212-TGC-T
gnomAD v4: 10-133539212-TGC-T
MyVariant Identifiers: chr10:g.135352717_135352723delinsTCTTG (hg19) chr10:g.133539213_133539219delinsTCTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539213_133539214del , CM000672.2:g.133539213_133539214del GRCh38
NC_000010.10:g.135352717_135352718del , CM000672.1:g.135352717_135352718del GRCh37
NC_000010.9:g.135202707_135202708del NCBI36
NG_008383.1:g.16851_16852del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1321_1358+1322del
Search 100 bp 5'
Search 100 bp 3'