Canonical Allele Identifier: CA1929221585
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780535C= , CM000672.2:g.94780535C= GRCh38
NC_000010.10:g.96540292C= , CM000672.1:g.96540292C= GRCh37
NC_000010.9:g.96530282C= NCBI36
NG_008384.2:g.22830C=
NG_008384.3:g.22855C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.518C= MANE Select ENSP00000360372.3:p.Ala173=
ENST00000645461.1:n.1571C=
ENST00000371321.7:c.518C= ENSP00000360372.3:p.Ala173=
ENST00000464755.1:c.1281C= ENSP00000483243.1:n.1281C=
NM_000769.2:c.518C= NP_000760.1:p.Ala173=
NM_000769.4:c.518C= MANE Select NP_000760.1:p.Ala173=