Canonical Allele Identifier: CA662022660

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1429451438
• gnomAD v3: 10-133526988-A-T
• gnomAD v4: 10-133526988-A-T
• MyVariant Identifiers: chr10:g.135340492A>T (hg19) ; chr10:g.133526988A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133526988A>T , CM000672.2:g.133526988A>T	GRCh38
NC_000010.10:g.135340492A>T , CM000672.1:g.135340492A>T	GRCh37
NC_000010.9:g.135190482A>T	NCBI36
NG_008383.1:g.4626A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463117.6:c.-40+115A>T	ENSP00000440689.1:n.-40+115A>T
ENST00000541261.1:c.-40+115A>T	ENSP00000437799.1:n.-40+115A>T