Canonical Allele Identifier: CA1929279875
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852746T= , CM000672.2:g.94852746T= GRCh38
NC_000010.10:g.96612503T= , CM000672.1:g.96612503T= GRCh37
NC_000010.9:g.96602493T= NCBI36
NG_008384.2:g.95041T=
NG_008384.3:g.95066T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1305T= MANE Select ENSP00000360372.3:p.Cys435=
ENST00000645461.1:n.2216T=
ENST00000371321.7:c.1305T= ENSP00000360372.3:p.Cys435=
ENST00000464755.1:c.2068T= ENSP00000483243.1:n.2068T=
NM_000769.2:c.1305T= NP_000760.1:p.Cys435=
NM_000769.4:c.1305T= MANE Select NP_000760.1:p.Cys435=