Canonical Allele Identifier: CA662011953

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1271016207
• MyVariant Identifiers: chr10:g.135352635T>C (hg19) ; chr10:g.133539131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133539131T>C , CM000672.2:g.133539131T>C	GRCh38
NC_000010.10:g.135352635T>C , CM000672.1:g.135352635T>C	GRCh37
NC_000010.9:g.135202625T>C	NCBI36
NG_008383.1:g.16769T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368520.1:n.1358+1239T>C