Canonical Allele Identifier: CA2610265240

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94852847-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852849del , CM000672.2:g.94852849del	GRCh38
NC_000010.10:g.96612606del , CM000672.1:g.96612606del	GRCh37
NC_000010.9:g.96602596del	NCBI36
NG_008384.2:g.95144del
NG_008384.3:g.95169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1408del MANE Select	ENSP00000360372.3:p.Thr470LeufsTer?
ENST00000645461.1:n.2319del
ENST00000371321.7:c.1408del	ENSP00000360372.3:p.Thr470LeufsTer?
ENST00000464755.1:c.2171del	ENSP00000483243.1:n.2171del
NM_000769.2:c.1408del	NP_000760.1:p.Thr470LeufsTer?
NM_000769.4:c.1408del MANE Select	NP_000760.1:p.Thr470LeufsTer?