Canonical Allele Identifier: CA1929222463
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781891C= , CM000672.2:g.94781891C= GRCh38
NC_000010.10:g.96541648C= , CM000672.1:g.96541648C= GRCh37
NC_000010.9:g.96531638C= NCBI36
NG_008384.2:g.24186C=
NG_008384.3:g.24211C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.713C= MANE Select ENSP00000360372.3:p.Ala238=
ENST00000645461.1:n.1766C=
ENST00000371321.7:c.713C= ENSP00000360372.3:p.Ala238=
ENST00000464755.1:c.1476C= ENSP00000483243.1:n.1476C=
NM_000769.2:c.713C= NP_000760.1:p.Ala238=
NM_000769.4:c.713C= MANE Select NP_000760.1:p.Ala238=