Canonical Allele Identifier: CA2574628708

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94852884-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852886del , CM000672.2:g.94852886del	GRCh38
NC_000010.10:g.96612643del , CM000672.1:g.96612643del	GRCh37
NC_000010.9:g.96602633del	NCBI36
NG_008384.2:g.95181del
NG_008384.3:g.95206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1445del MANE Select	ENSP00000360372.3:p.Phe482SerfsTer?
ENST00000645461.1:n.2356del
ENST00000371321.7:c.1445del	ENSP00000360372.3:p.Phe482SerfsTer?
ENST00000464755.1:c.2208del	ENSP00000483243.1:n.2208del
NM_000769.2:c.1445del	NP_000760.1:p.Phe482SerfsTer?
NM_000769.4:c.1445del MANE Select	NP_000760.1:p.Phe482SerfsTer?