Canonical Allele Identifier: CA2610264493
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780379_94780382del , CM000672.2:g.94780379_94780382del GRCh38
NC_000010.10:g.96540136_96540139del , CM000672.1:g.96540136_96540139del GRCh37
NC_000010.9:g.96530126_96530129del NCBI36
NG_008384.2:g.22674_22677del
NG_008384.3:g.22699_22702del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-120_482-117del MANE Select ENSP00000360372.3:n.482-120_482-117del
ENST00000645461.1:n.1535-120_1535-117del
ENST00000371321.7:c.482-120_482-117del ENSP00000360372.3:n.482-120_482-117del
ENST00000464755.1:c.1245-120_1245-117del ENSP00000483243.1:n.1245-120_1245-117del
NM_000769.2:c.482-120_482-117del NP_000760.1:n.482-120_482-117del
NM_000769.4:c.482-120_482-117del MANE Select NP_000760.1:n.482-120_482-117del