Canonical Allele Identifier: CA211680968
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1019684880

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780553G>T , CM000672.2:g.94780553G>T GRCh38
NC_000010.10:g.96540310G>T , CM000672.1:g.96540310G>T GRCh37
NC_000010.9:g.96530300G>T NCBI36
NG_008384.2:g.22848G>T
NG_008384.3:g.22873G>T

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.536G>T NP_000760.1:p.Cys179Phe
NM_000769.4:c.536G>T MANE Select NP_000760.1:p.Cys179Phe
ENST00000371321.7:c.536G>T ENSP00000360372.3:p.Cys179Phe
ENST00000464755.1:n.1299G>T ENSP00000483243.1:p.=