CYP2C19 cytochrome P450 family 2 subfamily C member 19

Information
Symbol
CYP2C19
Type
protein-coding
Description
cytochrome P450 family 2 subfamily C member 19
Entrez Gene ID
1557
Genome
hg19
Position
chr10:96,522,438-96,615,304
Genome
hg38
Position
chr10:94,762,681-94,855,547
MIM
124020 OMIM
HGNC
HGNC:2621 HGNC
Ensembl
ENSG00000165841 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
drug response 0 54
Likely benign; other 0 2
no classification for the single variant 0 12
not provided 1 0
Uncertain significance 0 32
Ranking
ClinVar
52
0
2
40
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CPCJ
SYNONYM CYP2C
SYNONYM CYPIIC17
SYNONYM CYPIIC19
SYNONYM P450C2C
SYNONYM P450IIC19
MIM 124020 OMIM
HGNC HGNC:2621 HGNC
Ensembl ENSG00000165841 Ensembl
AllianceGenome HGNC:2621
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000480405.2 hg38 chr10 94,762,681 94,776,450 13,770
ENST00000371321.9 hg38 chr10 94,762,681 94,855,547 92,867
ENST00000480405.2 hg19 chr10 96,522,438 96,536,207 13,770
ENST00000371321.9 hg19 chr10 96,522,438 96,615,304 92,867
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