Canonical Allele Identifier: CA2610264500
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780383del , CM000672.2:g.94780383del GRCh38
NC_000010.10:g.96540140del , CM000672.1:g.96540140del GRCh37
NC_000010.9:g.96530130del NCBI36
NG_008384.2:g.22678del
NG_008384.3:g.22703del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-116del MANE Select ENSP00000360372.3:n.482-116del
ENST00000645461.1:n.1535-116del
ENST00000371321.7:c.482-116del ENSP00000360372.3:n.482-116del
ENST00000464755.1:c.1245-116del ENSP00000483243.1:n.1245-116del
NM_000769.2:c.482-116del NP_000760.1:n.482-116del
NM_000769.4:c.482-116del MANE Select NP_000760.1:n.482-116del