Canonical Allele Identifier: CA1929279954
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852911C= , CM000672.2:g.94852911C= GRCh38
NC_000010.10:g.96612668C= , CM000672.1:g.96612668C= GRCh37
NC_000010.9:g.96602658C= NCBI36
NG_008384.2:g.95206C=
NG_008384.3:g.95231C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1470C= MANE Select ENSP00000360372.3:p.Val490=
ENST00000645461.1:n.2381C=
ENST00000371321.7:c.1470C= ENSP00000360372.3:p.Val490=
ENST00000464755.1:c.2233C= ENSP00000483243.1:n.2233C=
NM_000769.2:c.1470C= NP_000760.1:p.Val490=
NM_000769.4:c.1470C= MANE Select NP_000760.1:p.Val490=