Canonical Allele Identifier: CA1929222344

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781831A= , CM000672.2:g.94781831A=	GRCh38
NC_000010.10:g.96541588A= , CM000672.1:g.96541588A=	GRCh37
NC_000010.9:g.96531578A=	NCBI36
NG_008384.2:g.24126A=
NG_008384.3:g.24151A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.653A= MANE Select	ENSP00000360372.3:p.Asn218=
ENST00000645461.1:n.1706A=
ENST00000371321.7:c.653A=	ENSP00000360372.3:p.Asn218=
ENST00000464755.1:c.1416A=	ENSP00000483243.1:n.1416A=
NM_000769.2:c.653A=	NP_000760.1:p.Asn218=
NM_000769.4:c.653A= MANE Select	NP_000760.1:p.Asn218=