Canonical Allele Identifier: CA377669715
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96534930C>A (hg19) chr10:g.94775173C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775173C>A , CM000672.2:g.94775173C>A GRCh38
NC_000010.10:g.96534930C>A , CM000672.1:g.96534930C>A GRCh37
NC_000010.9:g.96524920C>A NCBI36
NG_008384.2:g.17468C>A
NG_008384.3:g.17493C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.284C>A MANE Select ENSP00000360372.3:p.Ser95Tyr
ENST00000645461.1:n.1337C>A
ENST00000371321.7:c.284C>A ENSP00000360372.3:p.Ser95Tyr
ENST00000464755.1:c.1047C>A ENSP00000483243.1:n.1047C>A
ENST00000480405.2:c.284C>A ENSP00000483847.1:p.Ser95Tyr
NM_000769.2:c.284C>A NP_000760.1:p.Ser95Tyr
NM_000769.4:c.284C>A MANE Select NP_000760.1:p.Ser95Tyr
Search 100 bp 5'
Search 100 bp 3'