Canonical Allele Identifier: CA5616883
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs775549674
ExAC: 10:96612713 GCT / G
gnomAD v2: 10-96612713-GCT-G
gnomAD v3: 10-94852956-GCT-G
gnomAD v4: 10-94852956-GCT-G
MyVariant Identifiers: chr10:g.96612714_96612715del (hg19) chr10:g.94852957_94852958del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852961_94852962del , CM000672.2:g.94852961_94852962del GRCh38
NC_000010.10:g.96612718_96612719del , CM000672.1:g.96612718_96612719del GRCh37
NC_000010.9:g.96602708_96602709del NCBI36
NG_008384.2:g.95256_95257del
NG_008384.3:g.95281_95282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*47_*48del MANE Select ENSP00000360372.3:n.*47_*48del
ENST00000645461.1:n.2431_2432del
ENST00000371321.7:c.*47_*48del ENSP00000360372.3:n.*47_*48del
ENST00000464755.1:c.2283_2284del ENSP00000483243.1:n.2283_2284del
NM_000769.2:c.*47_*48del NP_000760.1:n.*47_*48del
NM_000769.4:c.*47_*48del MANE Select NP_000760.1:n.*47_*48del
Search 100 bp 5'
Search 100 bp 3'