Canonical Allele Identifier: CA918736410
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs773529734

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762804delinsTACCCT , CM000672.2:g.94762804delinsTACCCT GRCh38
NG_008384.2:g.5099delinsTACCCT
NG_008384.3:g.5124delinsTACCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.99delinsTACCCT MANE Select ENSP00000360372.3:p.Pro35LeufsTer6
ENST00000371321.7:c.99delinsTACCCT ENSP00000360372.3:p.Pro35LeufsTer6
ENST00000464755.1:c.932-12254delinsTACCCT ENSP00000483243.1:n.932-12254delinsTACCCT
ENST00000480405.2:c.99delinsTACCCT ENSP00000483847.1:p.Pro35LeufsTer6
NM_000769.2:c.99delinsTACCCT NP_000760.1:p.Pro35LeufsTer6
NM_000769.4:c.99delinsTACCCT MANE Select NP_000760.1:p.Pro35LeufsTer6