Canonical Allele Identifier: CA595638634

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1564662988
• gnomAD v2: 10-96540385-ACAT-A
• gnomAD v4: 10-94780628-ACAT-A
• MyVariant Identifiers: chr10:g.96540386_96540388del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780631_94780633del , CM000672.2:g.94780631_94780633del	GRCh38
NC_000010.10:g.96540388_96540390del , CM000672.1:g.96540388_96540390del	GRCh37
NC_000010.9:g.96530378_96530380del	NCBI36
NG_008384.2:g.22926_22928del
NG_008384.3:g.22951_22953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.614_616del MANE Select	ENSP00000360372.3:p.Ile205del
ENST00000645461.1:n.1667_1669del
ENST00000371321.7:c.614_616del	ENSP00000360372.3:p.Ile205del
ENST00000464755.1:c.1377_1379del	ENSP00000483243.1:n.1377_1379del
NM_000769.2:c.614_616del	NP_000760.1:p.Ile205del
NM_000769.4:c.614_616del MANE Select	NP_000760.1:p.Ile205del