Canonical Allele Identifier: CA377670581
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780579G>T , CM000672.2:g.94780579G>T GRCh38
NC_000010.10:g.96540336G>T , CM000672.1:g.96540336G>T GRCh37
NC_000010.9:g.96530326G>T NCBI36
NG_008384.2:g.22874G>T
NG_008384.3:g.22899G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.562G>T MANE Select ENSP00000360372.3:p.Asp188Tyr
ENST00000645461.1:n.1615G>T
ENST00000371321.7:c.562G>T ENSP00000360372.3:p.Asp188Tyr
ENST00000464755.1:c.1325G>T ENSP00000483243.1:n.1325G>T
NM_000769.2:c.562G>T NP_000760.1:p.Asp188Tyr
NM_000769.4:c.562G>T MANE Select NP_000760.1:p.Asp188Tyr