Canonical Allele Identifier: CA377676086
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96612658T>G (hg19) chr10:g.94852901T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852901T>G , CM000672.2:g.94852901T>G GRCh38
NC_000010.10:g.96612658T>G , CM000672.1:g.96612658T>G GRCh37
NC_000010.9:g.96602648T>G NCBI36
NG_008384.2:g.95196T>G
NG_008384.3:g.95221T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1460T>G MANE Select ENSP00000360372.3:p.Phe487Cys
ENST00000645461.1:n.2371T>G
ENST00000371321.7:c.1460T>G ENSP00000360372.3:p.Phe487Cys
ENST00000464755.1:c.2223T>G ENSP00000483243.1:n.2223T>G
NM_000769.2:c.1460T>G NP_000760.1:p.Phe487Cys
NM_000769.4:c.1460T>G MANE Select NP_000760.1:p.Phe487Cys
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