Canonical Allele Identifier: CA1946822357
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs1851282016
gnomAD v4: 10-133527338-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527338A>T , CM000672.2:g.133527338A>T GRCh38
NC_000010.10:g.135340842A>T , CM000672.1:g.135340842A>T GRCh37
NC_000010.9:g.135190832A>T NCBI36
NG_008383.1:g.4976A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-39-19A>T ENSP00000440689.1:n.-39-19A>T
ENST00000541261.1:c.-39-19A>T ENSP00000437799.1:n.-39-19A>T
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