Canonical Allele Identifier: CA211697128
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs775981161
gnomAD v2: 10-96612764-C-A
gnomAD v3: 10-94853007-C-A
gnomAD v4: 10-94853007-C-A
MyVariant Identifiers: chr10:g.96612764C>A (hg19) chr10:g.94853007C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853007C>A , CM000672.2:g.94853007C>A GRCh38
NC_000010.10:g.96612764C>A , CM000672.1:g.96612764C>A GRCh37
NC_000010.9:g.96602754C>A NCBI36
NG_008384.2:g.95302C>A
NG_008384.3:g.95327C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*93C>A MANE Select ENSP00000360372.3:n.*93C>A
ENST00000645461.1:n.2477C>A
ENST00000371321.7:c.*93C>A ENSP00000360372.3:n.*93C>A
ENST00000464755.1:c.2329C>A ENSP00000483243.1:n.2329C>A
NM_000769.2:c.*93C>A NP_000760.1:n.*93C>A
NM_000769.4:c.*93C>A MANE Select NP_000760.1:n.*93C>A
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