Canonical Allele Identifier: CA1929222388
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781855_94781856delinsTC , CM000672.2:g.94781855_94781856delinsTC GRCh38
NC_000010.10:g.96541612_96541613delinsTC , CM000672.1:g.96541612_96541613delinsTC GRCh37
NC_000010.9:g.96531602_96531603delinsTC NCBI36
NG_008384.2:g.24150_24151delinsTC
NG_008384.3:g.24175_24176delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.677_678delinsTC MANE Select ENSP00000360372.3:p.Phe226=
ENST00000645461.1:n.1730_1731delinsTC
ENST00000371321.7:c.677_678delinsTC ENSP00000360372.3:p.Phe226=
ENST00000464755.1:c.1440_1441delinsTC ENSP00000483243.1:n.1440_1441delinsTC
NM_000769.2:c.677_678delinsTC NP_000760.1:p.Phe226=
NM_000769.4:c.677_678delinsTC MANE Select NP_000760.1:p.Phe226=
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Search 100 bp 3'