Canonical Allele Identifier: CA5616413
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs202170044

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775428C>G , CM000672.2:g.94775428C>G GRCh38
NC_000010.10:g.96535185C>G , CM000672.1:g.96535185C>G GRCh37
NC_000010.9:g.96525175C>G NCBI36
NG_008384.2:g.17723C>G
NG_008384.3:g.17748C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.370C>G MANE Select ENSP00000360372.3:p.Arg124Gly
ENST00000645461.1:n.1423C>G
ENST00000371321.7:c.370C>G ENSP00000360372.3:p.Arg124Gly
ENST00000464755.1:c.1133C>G ENSP00000483243.1:n.1133C>G
ENST00000480405.2:c.370C>G ENSP00000483847.1:p.Arg124Gly
NM_000769.2:c.370C>G NP_000760.1:p.Arg124Gly
NM_000769.4:c.370C>G MANE Select NP_000760.1:p.Arg124Gly