Canonical Allele Identifier: CA1929221590
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780542C= , CM000672.2:g.94780542C= GRCh38
NC_000010.10:g.96540299C= , CM000672.1:g.96540299C= GRCh37
NC_000010.9:g.96530289C= NCBI36
NG_008384.2:g.22837C=
NG_008384.3:g.22862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.525C= MANE Select ENSP00000360372.3:p.Cys175=
ENST00000645461.1:n.1578C=
ENST00000371321.7:c.525C= ENSP00000360372.3:p.Cys175=
ENST00000464755.1:c.1288C= ENSP00000483243.1:n.1288C=
NM_000769.2:c.525C= NP_000760.1:p.Cys175=
NM_000769.4:c.525C= MANE Select NP_000760.1:p.Cys175=
Search 100 bp 5'
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