Canonical Allele Identifier: CA377671300
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96541645T>G (hg19) chr10:g.94781888T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781888T>G , CM000672.2:g.94781888T>G GRCh38
NC_000010.10:g.96541645T>G , CM000672.1:g.96541645T>G GRCh37
NC_000010.9:g.96531635T>G NCBI36
NG_008384.2:g.24183T>G
NG_008384.3:g.24208T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.710T>G MANE Select ENSP00000360372.3:p.Leu237Arg
ENST00000645461.1:n.1763T>G
ENST00000371321.7:c.710T>G ENSP00000360372.3:p.Leu237Arg
ENST00000464755.1:c.1473T>G ENSP00000483243.1:n.1473T>G
NM_000769.2:c.710T>G NP_000760.1:p.Leu237Arg
NM_000769.4:c.710T>G MANE Select NP_000760.1:p.Leu237Arg
Search 100 bp 5'
Search 100 bp 3'