Canonical Allele Identifier: CA1929278235
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849918G= , CM000672.2:g.94849918G= GRCh38
NC_000010.10:g.96609675G= , CM000672.1:g.96609675G= GRCh37
NC_000010.9:g.96599665G= NCBI36
NG_008384.2:g.92213G=
NG_008384.3:g.92238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1151G= MANE Select ENSP00000360372.3:p.Gly384=
ENST00000645461.1:n.2062G=
ENST00000371321.7:c.1151G= ENSP00000360372.3:p.Gly384=
ENST00000464755.1:c.1914G= ENSP00000483243.1:n.1914G=
NM_000769.2:c.1151G= NP_000760.1:p.Gly384=
NM_000769.4:c.1151G= MANE Select NP_000760.1:p.Gly384=