Canonical Allele Identifier: CA1929278245
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849934T= , CM000672.2:g.94849934T= GRCh38
NC_000010.10:g.96609691T= , CM000672.1:g.96609691T= GRCh37
NC_000010.9:g.96599681T= NCBI36
NG_008384.2:g.92229T=
NG_008384.3:g.92254T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1167T= MANE Select ENSP00000360372.3:p.Thr389=
ENST00000645461.1:n.2078T=
ENST00000371321.7:c.1167T= ENSP00000360372.3:p.Thr389=
ENST00000464755.1:c.1930T= ENSP00000483243.1:n.1930T=
NM_000769.2:c.1167T= NP_000760.1:p.Thr389=
NM_000769.4:c.1167T= MANE Select NP_000760.1:p.Thr389=