Canonical Allele Identifier: CA2610265280

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94852992-ATGCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852993_94852997del , CM000672.2:g.94852993_94852997del	GRCh38
NC_000010.10:g.96612750_96612754del , CM000672.1:g.96612750_96612754del	GRCh37
NC_000010.9:g.96602740_96602744del	NCBI36
NG_008384.2:g.95288_95292del
NG_008384.3:g.95313_95317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*79_*83del MANE Select	ENSP00000360372.3:n.*79_*83del
ENST00000645461.1:n.2463_2467del
ENST00000371321.7:c.*79_*83del	ENSP00000360372.3:n.*79_*83del
ENST00000464755.1:c.2315_2319del	ENSP00000483243.1:n.2315_2319del
NM_000769.2:c.*79_*83del	NP_000760.1:n.*79_*83del
NM_000769.4:c.*79_*83del MANE Select	NP_000760.1:n.*79_*83del