Canonical Allele Identifier: CA211680922
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs28399510

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780519T>C , CM000672.2:g.94780519T>C GRCh38
NC_000010.10:g.96540276T>C , CM000672.1:g.96540276T>C GRCh37
NC_000010.9:g.96530266T>C NCBI36
NG_008384.2:g.22814T>C
NG_008384.3:g.22839T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.502T>C MANE Select ENSP00000360372.3:p.Phe168Leu
ENST00000645461.1:n.1555T>C
ENST00000371321.7:c.502T>C ENSP00000360372.3:p.Phe168Leu
ENST00000464755.1:c.1265T>C ENSP00000483243.1:n.1265T>C
NM_000769.2:c.502T>C NP_000760.1:p.Phe168Leu
NM_000769.4:c.502T>C MANE Select NP_000760.1:p.Phe168Leu