Canonical Allele Identifier: CA662011918
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1166257737
gnomAD v3: 10-133539100-C-A
gnomAD v4: 10-133539100-C-A
MyVariant Identifiers: chr10:g.135352604C>A (hg19) chr10:g.133539100C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539100C>A , CM000672.2:g.133539100C>A GRCh38
NC_000010.10:g.135352604C>A , CM000672.1:g.135352604C>A GRCh37
NC_000010.9:g.135202594C>A NCBI36
NG_008383.1:g.16738C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252945.8:c.*136C>A MANE Select ENSP00000252945.3:n.*136C>A
ENST00000252945.7:c.*136C>A ENSP00000252945.3:n.*136C>A
ENST00000368520.1:n.1358+1208C>A
ENST00000463117.6:c.*136C>A ENSP00000440689.1:n.*136C>A
ENST00000469258.1:n.714C>A
NM_000773.3:c.*136C>A NP_000764.1:n.*136C>A
NM_000773.4:c.*136C>A MANE Select NP_000764.1:n.*136C>A
Search 100 bp 5'
Search 100 bp 3'