Canonical Allele Identifier: CA597015884
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1445844611
gnomAD v2: 10-135340839-TA-T
gnomAD v3: 10-133527335-TA-T
gnomAD v4: 10-133527335-TA-T
MyVariant Identifiers: chr10:g.135340840del (hg19) chr10:g.133527336del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527340del , CM000672.2:g.133527340del GRCh38
NC_000010.10:g.135340844del , CM000672.1:g.135340844del GRCh37
NC_000010.9:g.135190834del NCBI36
NG_008383.1:g.4978del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-39-17del ENSP00000440689.1:n.-39-17del
ENST00000541261.1:c.-39-17del ENSP00000437799.1:n.-39-17del
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