Canonical Allele Identifier: CA377671174
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94781855-T-G
MyVariant Identifiers: chr10:g.96541612T>G (hg19) chr10:g.94781855T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781855T>G , CM000672.2:g.94781855T>G GRCh38
NC_000010.10:g.96541612T>G , CM000672.1:g.96541612T>G GRCh37
NC_000010.9:g.96531602T>G NCBI36
NG_008384.2:g.24150T>G
NG_008384.3:g.24175T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.677T>G MANE Select ENSP00000360372.3:p.Phe226Cys
ENST00000645461.1:n.1730T>G
ENST00000371321.7:c.677T>G ENSP00000360372.3:p.Phe226Cys
ENST00000464755.1:c.1440T>G ENSP00000483243.1:n.1440T>G
NM_000769.2:c.677T>G NP_000760.1:p.Phe226Cys
NM_000769.4:c.677T>G MANE Select NP_000760.1:p.Phe226Cys
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