Canonical Allele Identifier: CA662022694

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1350295521
• gnomAD v3: 10-133527140-C-G
• gnomAD v4: 10-133527140-C-G
• MyVariant Identifiers: chr10:g.135340644C>G (hg19) ; chr10:g.133527140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133527140C>G , CM000672.2:g.133527140C>G	GRCh38
NC_000010.10:g.135340644C>G , CM000672.1:g.135340644C>G	GRCh37
NC_000010.9:g.135190634C>G	NCBI36
NG_008383.1:g.4778C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463117.6:c.-39-217C>G	ENSP00000440689.1:n.-39-217C>G
ENST00000541261.1:c.-39-217C>G	ENSP00000437799.1:n.-39-217C>G