Canonical Allele Identifier: CA596749391
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v2: 10-135352716-TGCTCTTG-T
gnomAD v3: 10-133539212-TGCTCTTG-T
gnomAD v4: 10-133539212-TGCTCTTG-T
MyVariant Identifiers: chr10:g.135352717_135352723del (hg19) chr10:g.133539213_133539219del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539213_133539219del , CM000672.2:g.133539213_133539219del GRCh38
NC_000010.10:g.135352717_135352723del , CM000672.1:g.135352717_135352723del GRCh37
NC_000010.9:g.135202707_135202713del NCBI36
NG_008383.1:g.16851_16857del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1321_1358+1327del
Search 100 bp 5'
Search 100 bp 3'