Canonical Allele Identifier: CA2610264838
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.712del MANE Select ENSP00000360372.3:p.Ala238LeufsTer11
ENST00000645461.1:n.1765del
ENST00000371321.7:c.712del ENSP00000360372.3:p.Ala238LeufsTer11
ENST00000464755.1:c.1475del ENSP00000483243.1:n.1475del
NM_000769.2:c.712del NP_000760.1:p.Ala238LeufsTer11
NM_000769.4:c.712del MANE Select NP_000760.1:p.Ala238LeufsTer11