Canonical Allele Identifier: CA377671130
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079519
ClinVar RCV Id: RCV004367913
gnomAD v4: 10-94781842-A-G
MyVariant Identifiers: chr10:g.96541599A>G (hg19) chr10:g.94781842A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781842A>G , CM000672.2:g.94781842A>G GRCh38
NC_000010.10:g.96541599A>G , CM000672.1:g.96541599A>G GRCh37
NC_000010.9:g.96531589A>G NCBI36
NG_008384.2:g.24137A>G
NG_008384.3:g.24162A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.664A>G MANE Select ENSP00000360372.3:p.Ile222Val
ENST00000645461.1:n.1717A>G
ENST00000371321.7:c.664A>G ENSP00000360372.3:p.Ile222Val
ENST00000464755.1:c.1427A>G ENSP00000483243.1:n.1427A>G
NM_000769.2:c.664A>G NP_000760.1:p.Ile222Val
NM_000769.4:c.664A>G MANE Select NP_000760.1:p.Ile222Val
Search 100 bp 5'
Search 100 bp 3'