Canonical Allele Identifier: CA216859234
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs574206320
gnomAD v3: 10-133539172-GT-G
gnomAD v4: 10-133539172-GT-G
MyVariant Identifiers: chr10:g.135352677del (hg19) chr10:g.133539173del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539186del , CM000672.2:g.133539186del GRCh38
NC_000010.10:g.135352690del , CM000672.1:g.135352690del GRCh37
NC_000010.9:g.135202680del NCBI36
NG_008383.1:g.16824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1294del
Search 100 bp 5'
Search 100 bp 3'