Canonical Allele Identifier: CA377675759

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1200149422
• gnomAD v2: 10-96612500-T-G
• gnomAD v4: 10-94852743-T-G
• MyVariant Identifiers: chr10:g.96612500T>G (hg19) ; chr10:g.94852743T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852743T>G , CM000672.2:g.94852743T>G	GRCh38
NC_000010.10:g.96612500T>G , CM000672.1:g.96612500T>G	GRCh37
NC_000010.9:g.96602490T>G	NCBI36
NG_008384.2:g.95038T>G
NG_008384.3:g.95063T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.1302T>G MANE Select	ENSP00000360372.3:p.Ile434Met
ENST00000645461.1:n.2213T>G
ENST00000371321.7:c.1302T>G	ENSP00000360372.3:p.Ile434Met
ENST00000464755.1:c.2065T>G	ENSP00000483243.1:n.2065T>G
NM_000769.2:c.1302T>G	NP_000760.1:p.Ile434Met
NM_000769.4:c.1302T>G MANE Select	NP_000760.1:p.Ile434Met