Canonical Allele Identifier: CA596749397
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851447859
gnomAD v2: 10-135352718-C-CTTTTTTT
MyVariant Identifiers: chr10:g.135352718_135352719insTTTTTTT (hg19) chr10:g.133539214_133539215insTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539215_133539216insTTTTTTT , CM000672.2:g.133539215_133539216insTTTTTTT GRCh38
NC_000010.10:g.135352719_135352720insTTTTTTT , CM000672.1:g.135352719_135352720insTTTTTTT GRCh37
NC_000010.9:g.135202709_135202710insTTTTTTT NCBI36
NG_008383.1:g.16853_16854insTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1323_1358+1324insTTTTTTT
Search 100 bp 5'
Search 100 bp 3'