Canonical Allele Identifier: CA472245055
Gene: CYP2E1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.135345692C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133532188C>G , CM000672.2:g.133532188C>G GRCh38
NC_000010.10:g.135345692C>G , CM000672.1:g.135345692C>G GRCh37
NC_000010.9:g.135195682C>G NCBI36
NG_008383.1:g.9826C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.552C>G MANE Select ENSP00000252945.3:p.Leu184=
ENST00000252945.7:c.552C>G ENSP00000252945.3:p.Leu184=
ENST00000368520.1:n.613C>G
ENST00000418356.1:c.141C>G ENSP00000397299.1:p.Leu47=
ENST00000421586.5:c.291C>G ENSP00000412754.1:p.Leu97=
ENST00000463117.6:c.552C>G ENSP00000440689.1:p.Leu184=
ENST00000477500.5:n.448+454C>G
ENST00000541080.5:c.226+454C>G
NM_000773.3:c.552C>G NP_000764.1:p.Leu184=
NM_000773.4:c.552C>G MANE Select NP_000764.1:p.Leu184=
Search 100 bp 5'
Search 100 bp 3'