Canonical Allele Identifier: CA596749387
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v2: 10-135352712-G-GTTTTTTTTTT
MyVariant Identifiers: chr10:g.135352712_135352713insTTTTTTTTTT (hg19) chr10:g.133539208_133539209insTTTTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539212_133539213insTTTTTTTTTT , CM000672.2:g.133539212_133539213insTTTTTTTTTT GRCh38
NC_000010.10:g.135352716_135352717insTTTTTTTTTT , CM000672.1:g.135352716_135352717insTTTTTTTTTT GRCh37
NC_000010.9:g.135202706_135202707insTTTTTTTTTT NCBI36
NG_008383.1:g.16850_16851insTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1320_1358+1321insTTTTTTTTTT
Search 100 bp 5'
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