Canonical Allele Identifier: CA662022700

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1421570833
• gnomAD v3: 10-133527152-G-A
• gnomAD v4: 10-133527152-G-A
• MyVariant Identifiers: chr10:g.135340656G>A (hg19) ; chr10:g.133527152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133527152G>A , CM000672.2:g.133527152G>A	GRCh38
NC_000010.10:g.135340656G>A , CM000672.1:g.135340656G>A	GRCh37
NC_000010.9:g.135190646G>A	NCBI36
NG_008383.1:g.4790G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463117.6:c.-39-205G>A	ENSP00000440689.1:n.-39-205G>A
ENST00000541261.1:c.-39-205G>A	ENSP00000437799.1:n.-39-205G>A