Canonical Allele Identifier: CA918736759

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1564687599
• gnomAD v4: 10-94853027-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94853032del , CM000672.2:g.94853032del	GRCh38
NC_000010.10:g.96612789del , CM000672.1:g.96612789del	GRCh37
NC_000010.9:g.96602779del	NCBI36
NG_008384.2:g.95327del
NG_008384.3:g.95352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*118del MANE Select	ENSP00000360372.3:n.*118del
ENST00000645461.1:n.2502del
ENST00000371321.7:c.*118del	ENSP00000360372.3:n.*118del
ENST00000464755.1:c.2354del	ENSP00000483243.1:n.2354del
NM_000769.2:c.*118del	NP_000760.1:n.*118del
NM_000769.4:c.*118del MANE Select	NP_000760.1:n.*118del