Canonical Allele Identifier: CA597015883
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1247939614
gnomAD v2: 10-135340834-CATT-C
gnomAD v3: 10-133527330-CATT-C
gnomAD v4: 10-133527330-CATT-C
MyVariant Identifiers: chr10:g.135340835_135340837del (hg19) chr10:g.133527331_133527333del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527333_133527335del , CM000672.2:g.133527333_133527335del GRCh38
NC_000010.10:g.135340837_135340839del , CM000672.1:g.135340837_135340839del GRCh37
NC_000010.9:g.135190827_135190829del NCBI36
NG_008383.1:g.4971_4973del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-39-24_-39-22del ENSP00000440689.1:n.-39-24_-39-22del
ENST00000541261.1:c.-39-24_-39-22del ENSP00000437799.1:n.-39-24_-39-22del
Search 100 bp 5'
Search 100 bp 3'