Canonical Allele Identifier: CA1929280028
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853070T= , CM000672.2:g.94853070T= GRCh38
NC_000010.10:g.96612827T= , CM000672.1:g.96612827T= GRCh37
NC_000010.9:g.96602817T= NCBI36
NG_008384.2:g.95365T=
NG_008384.3:g.95390T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*156T= MANE Select ENSP00000360372.3:n.*156T=
ENST00000645461.1:n.2540T=
ENST00000371321.7:c.*156T= ENSP00000360372.3:n.*156T=
ENST00000464755.1:c.2392T= ENSP00000483243.1:n.2392T=
NM_000769.2:c.*156T= NP_000760.1:n.*156T=
NM_000769.4:c.*156T= MANE Select NP_000760.1:n.*156T=
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