Canonical Allele Identifier: CA470832925
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94850015-T-A
MyVariant Identifiers: chr10:g.96609772T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850015T>A , CM000672.2:g.94850015T>A GRCh38
NC_000010.10:g.96609772T>A , CM000672.1:g.96609772T>A GRCh37
NC_000010.9:g.96599762T>A NCBI36
NG_008384.2:g.92310T>A
NG_008384.3:g.92335T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1248T>A MANE Select ENSP00000360372.3:p.Gly416=
ENST00000645461.1:n.2159T>A
ENST00000371321.7:c.1248T>A ENSP00000360372.3:p.Gly416=
ENST00000464755.1:c.2011T>A ENSP00000483243.1:n.2011T>A
NM_000769.2:c.1248T>A NP_000760.1:p.Gly416=
NM_000769.4:c.1248T>A MANE Select NP_000760.1:p.Gly416=
Search 100 bp 5'
Search 100 bp 3'