Canonical Allele Identifier: CA1929218982
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775775C= , CM000672.2:g.94775775C= GRCh38
NC_000010.10:g.96535532C= , CM000672.1:g.96535532C= GRCh37
NC_000010.9:g.96525522C= NCBI36
NG_008384.2:g.18070C=
NG_008384.3:g.18095C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+236C= MANE Select ENSP00000360372.3:n.481+236C=
ENST00000645461.1:n.1534+236C=
ENST00000371321.7:c.481+236C= ENSP00000360372.3:n.481+236C=
ENST00000464755.1:c.1244+236C= ENSP00000483243.1:n.1244+236C=
ENST00000480405.2:c.*228C= ENSP00000483847.1:n.*228C=
NM_000769.2:c.481+236C= NP_000760.1:n.481+236C=
NM_000769.4:c.481+236C= MANE Select NP_000760.1:n.481+236C=
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