Canonical Allele Identifier: CA1929221583
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780529G= , CM000672.2:g.94780529G= GRCh38
NC_000010.10:g.96540286G= , CM000672.1:g.96540286G= GRCh37
NC_000010.9:g.96530276G= NCBI36
NG_008384.2:g.22824G=
NG_008384.3:g.22849G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.512G= MANE Select ENSP00000360372.3:p.Gly171=
ENST00000645461.1:n.1565G=
ENST00000371321.7:c.512G= ENSP00000360372.3:p.Gly171=
ENST00000464755.1:c.1275G= ENSP00000483243.1:n.1275G=
NM_000769.2:c.512G= NP_000760.1:p.Gly171=
NM_000769.4:c.512G= MANE Select NP_000760.1:p.Gly171=