Canonical Allele Identifier: CA596749358
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851447497
gnomAD v2: 10-135352704-TTTTG-T
gnomAD v3: 10-133539200-TTTTG-T
gnomAD v4: 10-133539200-TTTTG-T
MyVariant Identifiers: chr10:g.135352705_135352712delinsAGAG (hg19) chr10:g.133539201_133539208delinsAGAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539201_133539204del , CM000672.2:g.133539201_133539204del GRCh38
NC_000010.10:g.135352705_135352708del , CM000672.1:g.135352705_135352708del GRCh37
NC_000010.9:g.135202695_135202698del NCBI36
NG_008383.1:g.16839_16842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1309_1358+1312del
Search 100 bp 5'
Search 100 bp 3'