Canonical Allele Identifier: CA377675767

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1849673066
• MyVariant Identifiers: chr10:g.96612503T>G (hg19) ; chr10:g.94852746T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852746T>G , CM000672.2:g.94852746T>G	GRCh38
NC_000010.10:g.96612503T>G , CM000672.1:g.96612503T>G	GRCh37
NC_000010.9:g.96602493T>G	NCBI36
NG_008384.2:g.95041T>G
NG_008384.3:g.95066T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.1305T>G MANE Select	ENSP00000360372.3:p.Cys435Trp
ENST00000645461.1:n.2216T>G
ENST00000371321.7:c.1305T>G	ENSP00000360372.3:p.Cys435Trp
ENST00000464755.1:c.2068T>G	ENSP00000483243.1:n.2068T>G
NM_000769.2:c.1305T>G	NP_000760.1:p.Cys435Trp
NM_000769.4:c.1305T>G MANE Select	NP_000760.1:p.Cys435Trp