Canonical Allele Identifier: CA1929221599
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780567C= , CM000672.2:g.94780567C= GRCh38
NC_000010.10:g.96540324C= , CM000672.1:g.96540324C= GRCh37
NC_000010.9:g.96530314C= NCBI36
NG_008384.2:g.22862C=
NG_008384.3:g.22887C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.550C= MANE Select ENSP00000360372.3:p.Gln184=
ENST00000645461.1:n.1603C=
ENST00000371321.7:c.550C= ENSP00000360372.3:p.Gln184=
ENST00000464755.1:c.1313C= ENSP00000483243.1:n.1313C=
NM_000769.2:c.550C= NP_000760.1:p.Gln184=
NM_000769.4:c.550C= MANE Select NP_000760.1:p.Gln184=