Canonical Allele Identifier: CA1929221626

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780628A= , CM000672.2:g.94780628A=	GRCh38
NC_000010.10:g.96540385A= , CM000672.1:g.96540385A=	GRCh37
NC_000010.9:g.96530375A=	NCBI36
NG_008384.2:g.22923A=
NG_008384.3:g.22948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.611A= MANE Select	ENSP00000360372.3:p.Asn204=
ENST00000645461.1:n.1664A=
ENST00000371321.7:c.611A=	ENSP00000360372.3:p.Asn204=
ENST00000464755.1:c.1374A=	ENSP00000483243.1:n.1374A=
NM_000769.2:c.611A=	NP_000760.1:p.Asn204=
NM_000769.4:c.611A= MANE Select	NP_000760.1:p.Asn204=