Canonical Allele Identifier: CA662012297
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1351764336
MyVariant Identifiers: chr10:g.135352782G>T (hg19) chr10:g.133539278G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539278G>T , CM000672.2:g.133539278G>T GRCh38
NC_000010.10:g.135352782G>T , CM000672.1:g.135352782G>T GRCh37
NC_000010.9:g.135202772G>T NCBI36
NG_008383.1:g.16916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368520.1:n.1358+1386G>T
Search 100 bp 5'
Search 100 bp 3'