Canonical Allele Identifier: CA1929222380

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781854T= , CM000672.2:g.94781854T=	GRCh38
NC_000010.10:g.96541611T= , CM000672.1:g.96541611T=	GRCh37
NC_000010.9:g.96531601T=	NCBI36
NG_008384.2:g.24149T=
NG_008384.3:g.24174T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.676T= MANE Select	ENSP00000360372.3:p.Phe226=
ENST00000645461.1:n.1729T=
ENST00000371321.7:c.676T=	ENSP00000360372.3:p.Phe226=
ENST00000464755.1:c.1439T=	ENSP00000483243.1:n.1439T=
NM_000769.2:c.676T=	NP_000760.1:p.Phe226=
NM_000769.4:c.676T= MANE Select	NP_000760.1:p.Phe226=