Canonical Allele Identifier: CA2610265213

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94852663-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852667_94852668del , CM000672.2:g.94852667_94852668del	GRCh38
NC_000010.10:g.96612424_96612425del , CM000672.1:g.96612424_96612425del	GRCh37
NC_000010.9:g.96602414_96602415del	NCBI36
NG_008384.2:g.94962_94963del
NG_008384.3:g.94987_94988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-66_1292-65del MANE Select	ENSP00000360372.3:n.1292-66_1292-65del
ENST00000645461.1:n.2203-66_2203-65del
ENST00000371321.7:c.1292-66_1292-65del	ENSP00000360372.3:n.1292-66_1292-65del
ENST00000464755.1:c.2055-66_2055-65del	ENSP00000483243.1:n.2055-66_2055-65del
NM_000769.2:c.1292-66_1292-65del	NP_000760.1:n.1292-66_1292-65del
NM_000769.4:c.1292-66_1292-65del MANE Select	NP_000760.1:n.1292-66_1292-65del