Canonical Allele Identifier: CA377675849
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1253000953
gnomAD v3: 10-94852789-A-C
gnomAD v4: 10-94852789-A-C
MyVariant Identifiers: chr10:g.96612546A>C (hg19) chr10:g.94852789A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852789A>C , CM000672.2:g.94852789A>C GRCh38
NC_000010.10:g.96612546A>C , CM000672.1:g.96612546A>C GRCh37
NC_000010.9:g.96602536A>C NCBI36
NG_008384.2:g.95084A>C
NG_008384.3:g.95109A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1348A>C MANE Select ENSP00000360372.3:p.Thr450Pro
ENST00000645461.1:n.2259A>C
ENST00000371321.7:c.1348A>C ENSP00000360372.3:p.Thr450Pro
ENST00000464755.1:c.2111A>C ENSP00000483243.1:n.2111A>C
NM_000769.2:c.1348A>C NP_000760.1:p.Thr450Pro
NM_000769.4:c.1348A>C MANE Select NP_000760.1:p.Thr450Pro
Search 100 bp 5'
Search 100 bp 3'