Canonical Allele Identifier: CA1929222456
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781890G= , CM000672.2:g.94781890G= GRCh38
NC_000010.10:g.96541647G= , CM000672.1:g.96541647G= GRCh37
NC_000010.9:g.96531637G= NCBI36
NG_008384.2:g.24185G=
NG_008384.3:g.24210G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.712G= MANE Select ENSP00000360372.3:p.Ala238=
ENST00000645461.1:n.1765G=
ENST00000371321.7:c.712G= ENSP00000360372.3:p.Ala238=
ENST00000464755.1:c.1475G= ENSP00000483243.1:n.1475G=
NM_000769.2:c.712G= NP_000760.1:p.Ala238=
NM_000769.4:c.712G= MANE Select NP_000760.1:p.Ala238=