Canonical Allele Identifier: CA1929221624
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780625A= , CM000672.2:g.94780625A= GRCh38
NC_000010.10:g.96540382A= , CM000672.1:g.96540382A= GRCh37
NC_000010.9:g.96530372A= NCBI36
NG_008384.2:g.22920A=
NG_008384.3:g.22945A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.608A= MANE Select ENSP00000360372.3:p.Glu203=
ENST00000645461.1:n.1661A=
ENST00000371321.7:c.608A= ENSP00000360372.3:p.Glu203=
ENST00000464755.1:c.1371A= ENSP00000483243.1:n.1371A=
NM_000769.2:c.608A= NP_000760.1:p.Glu203=
NM_000769.4:c.608A= MANE Select NP_000760.1:p.Glu203=
Search 100 bp 5'
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