Canonical Allele Identifier: CA1929279924
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852839C= , CM000672.2:g.94852839C= GRCh38
NC_000010.10:g.96612596C= , CM000672.1:g.96612596C= GRCh37
NC_000010.9:g.96602586C= NCBI36
NG_008384.2:g.95134C=
NG_008384.3:g.95159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1398C= MANE Select ENSP00000360372.3:p.Asp466=
ENST00000645461.1:n.2309C=
ENST00000371321.7:c.1398C= ENSP00000360372.3:p.Asp466=
ENST00000464755.1:c.2161C= ENSP00000483243.1:n.2161C=
NM_000769.2:c.1398C= NP_000760.1:p.Asp466=
NM_000769.4:c.1398C= MANE Select NP_000760.1:p.Asp466=