Canonical Allele Identifier: CA2611613515
Gene: CYP2E1 HGNC NCBI

Linked Data

gnomAD v4: 10-133526767-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133526767T>C , CM000672.2:g.133526767T>C GRCh38
NC_000010.10:g.135340271T>C , CM000672.1:g.135340271T>C GRCh37
NC_000010.9:g.135190261T>C NCBI36
NG_008383.1:g.4405T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463117.6:c.-117-29T>C ENSP00000440689.1:n.-117-29T>C
ENST00000541261.1:c.-117-29T>C ENSP00000437799.1:n.-117-29T>C
XR_001747676.2:n.39A>G
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