Canonical Allele Identifier: CA5616303
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762804C= , CM000672.2:g.94762804C= GRCh38
NG_008384.2:g.5099C=
NG_008384.3:g.5124C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.99C= MANE Select ENSP00000360372.3:p.Pro33=
ENST00000371321.7:c.99C= ENSP00000360372.3:p.Pro33=
ENST00000464755.1:c.932-12254C= ENSP00000483243.1:n.932-12254C=
ENST00000480405.2:c.99C= ENSP00000483847.1:p.Pro33=
NM_000769.2:c.99C= NP_000760.1:p.Pro33=
NM_000769.4:c.99C= MANE Select NP_000760.1:p.Pro33=