Canonical Allele Identifier: CA1929218759
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775408G= , CM000672.2:g.94775408G= GRCh38
NC_000010.10:g.96535165G= , CM000672.1:g.96535165G= GRCh37
NC_000010.9:g.96525155G= NCBI36
NG_008384.2:g.17703G=
NG_008384.3:g.17728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.350G= MANE Select ENSP00000360372.3:p.Gly117=
ENST00000645461.1:n.1403G=
ENST00000371321.7:c.350G= ENSP00000360372.3:p.Gly117=
ENST00000464755.1:c.1113G= ENSP00000483243.1:n.1113G=
ENST00000480405.2:c.350G= ENSP00000483847.1:p.Gly117=
NM_000769.2:c.350G= NP_000760.1:p.Gly117=
NM_000769.4:c.350G= MANE Select NP_000760.1:p.Gly117=