Canonical Allele Identifier: CA1929278299
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850012A= , CM000672.2:g.94850012A= GRCh38
NC_000010.10:g.96609769A= , CM000672.1:g.96609769A= GRCh37
NC_000010.9:g.96599759A= NCBI36
NG_008384.2:g.92307A=
NG_008384.3:g.92332A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1245A= MANE Select ENSP00000360372.3:p.Glu415=
ENST00000645461.1:n.2156A=
ENST00000371321.7:c.1245A= ENSP00000360372.3:p.Glu415=
ENST00000464755.1:c.2008A= ENSP00000483243.1:n.2008A=
NM_000769.2:c.1245A= NP_000760.1:p.Glu415=
NM_000769.4:c.1245A= MANE Select NP_000760.1:p.Glu415=