Canonical Allele Identifier: CA670196152
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1373857547
gnomAD v3: 10-94852558-AC-A
gnomAD v4: 10-94852558-AC-A
MyVariant Identifiers: chr10:g.96612316del (hg19) chr10:g.94852559del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852561del , CM000672.2:g.94852561del GRCh38
NC_000010.10:g.96612318del , CM000672.1:g.96612318del GRCh37
NC_000010.9:g.96602308del NCBI36
NG_008384.2:g.94856del
NG_008384.3:g.94881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-172del MANE Select ENSP00000360372.3:n.1292-172del
ENST00000645461.1:n.2203-172del
ENST00000371321.7:c.1292-172del ENSP00000360372.3:n.1292-172del
ENST00000464755.1:c.2055-172del ENSP00000483243.1:n.2055-172del
NM_000769.2:c.1292-172del NP_000760.1:n.1292-172del
NM_000769.4:c.1292-172del MANE Select NP_000760.1:n.1292-172del
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