Canonical Allele Identifier: CA216856363
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs978146509
gnomAD v3: 10-133527164-T-C
gnomAD v4: 10-133527164-T-C
MyVariant Identifiers: chr10:g.135340668T>C (hg19) chr10:g.133527164T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133527164T>C , CM000672.2:g.133527164T>C GRCh38
NC_000010.10:g.135340668T>C , CM000672.1:g.135340668T>C GRCh37
NC_000010.9:g.135190658T>C NCBI36
NG_008383.1:g.4802T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463117.6:c.-39-193T>C ENSP00000440689.1:n.-39-193T>C
ENST00000541261.1:c.-39-193T>C ENSP00000437799.1:n.-39-193T>C
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