Canonical Allele Identifier: CA377670558
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780568A>G , CM000672.2:g.94780568A>G GRCh38
NC_000010.10:g.96540325A>G , CM000672.1:g.96540325A>G GRCh37
NC_000010.9:g.96530315A>G NCBI36
NG_008384.2:g.22863A>G
NG_008384.3:g.22888A>G

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.551A>G NP_000760.1:p.Gln184Arg
NM_000769.4:c.551A>G MANE Select NP_000760.1:p.Gln184Arg
ENST00000371321.7:c.551A>G ENSP00000360372.3:p.Gln184Arg
ENST00000464755.1:n.1314A>G ENSP00000483243.1:p.=