Canonical Allele Identifier: CA1929218782

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775446A= , CM000672.2:g.94775446A=	GRCh38
NC_000010.10:g.96535203A= , CM000672.1:g.96535203A=	GRCh37
NC_000010.9:g.96525193A=	NCBI36
NG_008384.2:g.17741A=
NG_008384.3:g.17766A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.388A= MANE Select	ENSP00000360372.3:p.Thr130=
ENST00000645461.1:n.1441A=
ENST00000371321.7:c.388A=	ENSP00000360372.3:p.Thr130=
ENST00000464755.1:c.1151A=	ENSP00000483243.1:n.1151A=
ENST00000480405.2:c.388A=	ENSP00000483847.1:p.Thr130=
NM_000769.2:c.388A=	NP_000760.1:p.Thr130=
NM_000769.4:c.388A= MANE Select	NP_000760.1:p.Thr130=