Canonical Allele Identifier: CA1929222220

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1564663313

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781729T>G , CM000672.2:g.94781729T>G	GRCh38
NC_000010.10:g.96541486T>G , CM000672.1:g.96541486T>G	GRCh37
NC_000010.9:g.96531476T>G	NCBI36
NG_008384.2:g.24024T>G
NG_008384.3:g.24049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.643-92T>G MANE Select	ENSP00000360372.3:n.643-92T>G
ENST00000645461.1:n.1696-92T>G
ENST00000371321.7:c.643-92T>G	ENSP00000360372.3:n.643-92T>G
ENST00000464755.1:c.1406-92T>G	ENSP00000483243.1:n.1406-92T>G
NM_000769.2:c.643-92T>G	NP_000760.1:n.643-92T>G
NM_000769.4:c.643-92T>G MANE Select	NP_000760.1:n.643-92T>G