Canonical Allele Identifier: CA5616684
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs775646392
ExAC: 10:96602587 T / C
gnomAD v2: 10-96602587-T-C
gnomAD v4: 10-94842830-T-C
MyVariant Identifiers: chr10:g.96602587T>C (hg19) chr10:g.94842830T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842830T>C , CM000672.2:g.94842830T>C GRCh38
NC_000010.10:g.96602587T>C , CM000672.1:g.96602587T>C GRCh37
NC_000010.9:g.96592577T>C NCBI36
NG_008384.2:g.85125T>C
NG_008384.3:g.85150T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.962-7T>C MANE Select ENSP00000360372.3:n.962-7T>C
ENST00000645461.1:n.1873-7T>C
ENST00000371321.7:c.962-7T>C ENSP00000360372.3:n.962-7T>C
ENST00000464755.1:c.1725-7T>C ENSP00000483243.1:n.1725-7T>C
NM_000769.2:c.962-7T>C NP_000760.1:n.962-7T>C
NM_000769.4:c.962-7T>C MANE Select NP_000760.1:n.962-7T>C
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