Canonical Allele Identifier: CA596749323
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1462914326
gnomAD v2: 10-135352688-TTTATTTTTG-T
gnomAD v3: 10-133539184-TTTATTTTTG-T
gnomAD v4: 10-133539184-TTTATTTTTG-T
MyVariant Identifiers: chr10:g.135352689_135352697del (hg19) chr10:g.133539185_133539193del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539187_133539195del , CM000672.2:g.133539187_133539195del GRCh38
NC_000010.10:g.135352691_135352699del , CM000672.1:g.135352691_135352699del GRCh37
NC_000010.9:g.135202681_135202689del NCBI36
NG_008383.1:g.16825_16833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1295_1358+1303del
Search 100 bp 5'
Search 100 bp 3'