Canonical Allele Identifier: CA1929218784
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775448G= , CM000672.2:g.94775448G= GRCh38
NC_000010.10:g.96535205G= , CM000672.1:g.96535205G= GRCh37
NC_000010.9:g.96525195G= NCBI36
NG_008384.2:g.17743G=
NG_008384.3:g.17768G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.390G= MANE Select ENSP00000360372.3:p.Thr130=
ENST00000645461.1:n.1443G=
ENST00000371321.7:c.390G= ENSP00000360372.3:p.Thr130=
ENST00000464755.1:c.1153G= ENSP00000483243.1:n.1153G=
ENST00000480405.2:c.390G= ENSP00000483847.1:p.Thr130=
NM_000769.2:c.390G= NP_000760.1:p.Thr130=
NM_000769.4:c.390G= MANE Select NP_000760.1:p.Thr130=