Canonical Allele Identifier: CA1929271636

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94842830T= , CM000672.2:g.94842830T=	GRCh38
NC_000010.10:g.96602587T= , CM000672.1:g.96602587T=	GRCh37
NC_000010.9:g.96592577T=	NCBI36
NG_008384.2:g.85125T=
NG_008384.3:g.85150T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.962-7T= MANE Select	ENSP00000360372.3:n.962-7T=
ENST00000645461.1:n.1873-7T=
ENST00000371321.7:c.962-7T=	ENSP00000360372.3:n.962-7T=
ENST00000464755.1:c.1725-7T=	ENSP00000483243.1:n.1725-7T=
NM_000769.2:c.962-7T=	NP_000760.1:n.962-7T=
NM_000769.4:c.962-7T= MANE Select	NP_000760.1:n.962-7T=