Canonical Allele Identifier: CA596749320
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v2: 10-135352682-T-TTTTTTTTA
MyVariant Identifiers: chr10:g.135352682_135352683insTTTTTTTA (hg19) chr10:g.133539178_133539179insTTTTTTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539185_133539186insATTTTTTT , CM000672.2:g.133539185_133539186insATTTTTTT GRCh38
NC_000010.10:g.135352689_135352690insATTTTTTT , CM000672.1:g.135352689_135352690insATTTTTTT GRCh37
NC_000010.9:g.135202679_135202680insATTTTTTT NCBI36
NG_008383.1:g.16823_16824insATTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1293_1358+1294insATTTTTTT
Search 100 bp 5'
Search 100 bp 3'