Canonical Allele Identifier: CA1929218599
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775129T= , CM000672.2:g.94775129T= GRCh38
NC_000010.10:g.96534886T= , CM000672.1:g.96534886T= GRCh37
NC_000010.9:g.96524876T= NCBI36
NG_008384.2:g.17424T=
NG_008384.3:g.17449T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.240T= MANE Select ENSP00000360372.3:p.Tyr80=
ENST00000645461.1:n.1293T=
ENST00000371321.7:c.240T= ENSP00000360372.3:p.Tyr80=
ENST00000464755.1:c.1003T= ENSP00000483243.1:p.Ter335=
ENST00000480405.2:c.240T= ENSP00000483847.1:p.Tyr80=
NM_000769.2:c.240T= NP_000760.1:p.Tyr80=
NM_000769.4:c.240T= MANE Select NP_000760.1:p.Tyr80=