Canonical Allele Identifier: CA931395206
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849679675
gnomAD v3: 10-94853047-A-C
gnomAD v4: 10-94853047-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853047A>C , CM000672.2:g.94853047A>C GRCh38
NC_000010.10:g.96612804A>C , CM000672.1:g.96612804A>C GRCh37
NC_000010.9:g.96602794A>C NCBI36
NG_008384.2:g.95342A>C
NG_008384.3:g.95367A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*133A>C MANE Select ENSP00000360372.3:n.*133A>C
ENST00000645461.1:n.2517A>C
ENST00000371321.7:c.*133A>C ENSP00000360372.3:n.*133A>C
ENST00000464755.1:c.2369A>C ENSP00000483243.1:n.2369A>C
NM_000769.2:c.*133A>C NP_000760.1:n.*133A>C
NM_000769.4:c.*133A>C MANE Select NP_000760.1:n.*133A>C
Search 100 bp 5'
Search 100 bp 3'