Canonical Allele Identifier: CA211696759
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1042611883
gnomAD v2: 10-96612511-A-T
gnomAD v3: 10-94852754-A-T
gnomAD v4: 10-94852754-A-T
MyVariant Identifiers: chr10:g.96612511A>T (hg19) chr10:g.94852754A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852754A>T , CM000672.2:g.94852754A>T GRCh38
NC_000010.10:g.96612511A>T , CM000672.1:g.96612511A>T GRCh37
NC_000010.9:g.96602501A>T NCBI36
NG_008384.2:g.95049A>T
NG_008384.3:g.95074A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1313A>T MANE Select ENSP00000360372.3:p.Glu438Val
ENST00000645461.1:n.2224A>T
ENST00000371321.7:c.1313A>T ENSP00000360372.3:p.Glu438Val
ENST00000464755.1:c.2076A>T ENSP00000483243.1:n.2076A>T
NM_000769.2:c.1313A>T NP_000760.1:p.Glu438Val
NM_000769.4:c.1313A>T MANE Select NP_000760.1:p.Glu438Val
Search 100 bp 5'
Search 100 bp 3'