Canonical Allele Identifier: CA596746493

Gene: CYP2E1

Linked Data

• dbSNP Id: rs1216005268
• gnomAD v2: 10-135340715-C-T
• gnomAD v4: 10-133527211-C-T
• MyVariant Identifiers: chr10:g.135340715C>T (hg19) ; chr10:g.133527211C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133527211C>T , CM000672.2:g.133527211C>T	GRCh38
NC_000010.10:g.135340715C>T , CM000672.1:g.135340715C>T	GRCh37
NC_000010.9:g.135190705C>T	NCBI36
NG_008383.1:g.4849C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463117.6:c.-39-146C>T	ENSP00000440689.1:n.-39-146C>T
ENST00000541261.1:c.-39-146C>T	ENSP00000437799.1:n.-39-146C>T