Canonical Allele Identifier: CA1929279900
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852789A= , CM000672.2:g.94852789A= GRCh38
NC_000010.10:g.96612546A= , CM000672.1:g.96612546A= GRCh37
NC_000010.9:g.96602536A= NCBI36
NG_008384.2:g.95084A=
NG_008384.3:g.95109A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1348A= MANE Select ENSP00000360372.3:p.Thr450=
ENST00000645461.1:n.2259A=
ENST00000371321.7:c.1348A= ENSP00000360372.3:p.Thr450=
ENST00000464755.1:c.2111A= ENSP00000483243.1:n.2111A=
NM_000769.2:c.1348A= NP_000760.1:p.Thr450=
NM_000769.4:c.1348A= MANE Select NP_000760.1:p.Thr450=