Canonical Allele Identifier: CA1929279955
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852913G= , CM000672.2:g.94852913G= GRCh38
NC_000010.10:g.96612670G= , CM000672.1:g.96612670G= GRCh37
NC_000010.9:g.96602660G= NCBI36
NG_008384.2:g.95208G=
NG_008384.3:g.95233G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1472G= MANE Select ENSP00000360372.3:p.Ter491=
ENST00000645461.1:n.2383G=
ENST00000371321.7:c.1472G= ENSP00000360372.3:p.Ter491=
ENST00000464755.1:c.2235G= ENSP00000483243.1:n.2235G=
NM_000769.2:c.1472G= NP_000760.1:p.Ter491=
NM_000769.4:c.1472G= MANE Select NP_000760.1:p.Ter491=