Canonical Allele Identifier: CA1929221617
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780605C= , CM000672.2:g.94780605C= GRCh38
NC_000010.10:g.96540362C= , CM000672.1:g.96540362C= GRCh37
NC_000010.9:g.96530352C= NCBI36
NG_008384.2:g.22900C=
NG_008384.3:g.22925C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.588C= MANE Select ENSP00000360372.3:p.Asn196=
ENST00000645461.1:n.1641C=
ENST00000371321.7:c.588C= ENSP00000360372.3:p.Asn196=
ENST00000464755.1:c.1351C= ENSP00000483243.1:n.1351C=
NM_000769.2:c.588C= NP_000760.1:p.Asn196=
NM_000769.4:c.588C= MANE Select NP_000760.1:p.Asn196=