Canonical Allele Identifier: CA2610265122

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94850203-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850203_94850204insCT , CM000672.2:g.94850203_94850204insCT	GRCh38
NC_000010.10:g.96609960_96609961insCT , CM000672.1:g.96609960_96609961insCT	GRCh37
NC_000010.9:g.96599950_96599951insCT	NCBI36
NG_008384.2:g.92498_92499insCT
NG_008384.3:g.92523_92524insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+145_1291+146insCT MANE Select	ENSP00000360372.3:n.1291+145_1291+146insCT
ENST00000645461.1:n.2202+145_2202+146insCT
ENST00000371321.7:c.1291+145_1291+146insCT	ENSP00000360372.3:n.1291+145_1291+146insCT
ENST00000464755.1:c.2054+145_2054+146insCT	ENSP00000483243.1:n.2054+145_2054+146insCT
NM_000769.2:c.1291+145_1291+146insCT	NP_000760.1:n.1291+145_1291+146insCT
NM_000769.4:c.1291+145_1291+146insCT MANE Select	NP_000760.1:n.1291+145_1291+146insCT