Canonical Allele Identifier: CA377669740
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1288601658

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775185A>G , CM000672.2:g.94775185A>G GRCh38
NC_000010.10:g.96534942A>G , CM000672.1:g.96534942A>G GRCh37
NC_000010.9:g.96524932A>G NCBI36
NG_008384.2:g.17480A>G
NG_008384.3:g.17505A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.296A>G MANE Select ENSP00000360372.3:p.His99Arg
ENST00000645461.1:n.1349A>G
ENST00000371321.7:c.296A>G ENSP00000360372.3:p.His99Arg
ENST00000464755.1:c.1059A>G ENSP00000483243.1:n.1059A>G
ENST00000480405.2:c.296A>G ENSP00000483847.1:p.His99Arg
NM_000769.2:c.296A>G NP_000760.1:p.His99Arg
NM_000769.4:c.296A>G MANE Select NP_000760.1:p.His99Arg