Canonical Allele Identifier: CA2610264839
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781895del , CM000672.2:g.94781895del GRCh38
NC_000010.10:g.96541652del , CM000672.1:g.96541652del GRCh37
NC_000010.9:g.96531642del NCBI36
NG_008384.2:g.24190del
NG_008384.3:g.24215del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.717del MANE Select ENSP00000360372.3:p.Phe239LeufsTer10
ENST00000645461.1:n.1770del
ENST00000371321.7:c.717del ENSP00000360372.3:p.Phe239LeufsTer10
ENST00000464755.1:c.1480del ENSP00000483243.1:n.1480del
NM_000769.2:c.717del NP_000760.1:p.Phe239LeufsTer10
NM_000769.4:c.717del MANE Select NP_000760.1:p.Phe239LeufsTer10