Canonical Allele Identifier: CA211697174
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs903529348
gnomAD v2: 10-96612789-C-A
gnomAD v3: 10-94853032-C-A
gnomAD v4: 10-94853032-C-A
MyVariant Identifiers: chr10:g.96612789C>A (hg19) chr10:g.94853032C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853032C>A , CM000672.2:g.94853032C>A GRCh38
NC_000010.10:g.96612789C>A , CM000672.1:g.96612789C>A GRCh37
NC_000010.9:g.96602779C>A NCBI36
NG_008384.2:g.95327C>A
NG_008384.3:g.95352C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*118C>A MANE Select ENSP00000360372.3:n.*118C>A
ENST00000645461.1:n.2502C>A
ENST00000371321.7:c.*118C>A ENSP00000360372.3:n.*118C>A
ENST00000464755.1:c.2354C>A ENSP00000483243.1:n.2354C>A
NM_000769.2:c.*118C>A NP_000760.1:n.*118C>A
NM_000769.4:c.*118C>A MANE Select NP_000760.1:n.*118C>A
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