Canonical Allele Identifier: CA5616470
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs776181631

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780493A>G , CM000672.2:g.94780493A>G GRCh38
NC_000010.10:g.96540250A>G , CM000672.1:g.96540250A>G GRCh37
NC_000010.9:g.96530240A>G NCBI36
NG_008384.2:g.22788A>G
NG_008384.3:g.22813A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-6A>G MANE Select ENSP00000360372.3:p.=
ENST00000371321.7:c.482-6A>G ENSP00000360372.3:p.=
ENST00000464755.1:n.1245-6A>G ENSP00000483243.1:p.=
NM_000769.2:c.482-6A>G NP_000760.1:p.=
NM_000769.4:c.482-6A>G MANE Select NP_000760.1:p.=