Canonical Allele Identifier: CA1929279881
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852757G= , CM000672.2:g.94852757G= GRCh38
NC_000010.10:g.96612514G= , CM000672.1:g.96612514G= GRCh37
NC_000010.9:g.96602504G= NCBI36
NG_008384.2:g.95052G=
NG_008384.3:g.95077G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1316G= MANE Select ENSP00000360372.3:p.Gly439=
ENST00000645461.1:n.2227G=
ENST00000371321.7:c.1316G= ENSP00000360372.3:p.Gly439=
ENST00000464755.1:c.2079G= ENSP00000483243.1:n.2079G=
NM_000769.2:c.1316G= NP_000760.1:p.Gly439=
NM_000769.4:c.1316G= MANE Select NP_000760.1:p.Gly439=