Canonical Allele Identifier: CA1929278296
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850006G= , CM000672.2:g.94850006G= GRCh38
NC_000010.10:g.96609763G= , CM000672.1:g.96609763G= GRCh37
NC_000010.9:g.96599753G= NCBI36
NG_008384.2:g.92301G=
NG_008384.3:g.92326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1239G= MANE Select ENSP00000360372.3:p.Leu413=
ENST00000645461.1:n.2150G=
ENST00000371321.7:c.1239G= ENSP00000360372.3:p.Leu413=
ENST00000464755.1:c.2002G= ENSP00000483243.1:n.2002G=
NM_000769.2:c.1239G= NP_000760.1:p.Leu413=
NM_000769.4:c.1239G= MANE Select NP_000760.1:p.Leu413=