Canonical Allele Identifier: CA1929222856

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782158A= , CM000672.2:g.94782158A=	GRCh38
NC_000010.10:g.96541915A= , CM000672.1:g.96541915A=	GRCh37
NC_000010.9:g.96531905A=	NCBI36
NG_008384.2:g.24453A=
NG_008384.3:g.24478A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+161A= MANE Select	ENSP00000360372.3:n.819+161A=
ENST00000645461.1:n.1872+161A=
ENST00000371321.7:c.819+161A=	ENSP00000360372.3:n.819+161A=
ENST00000464755.1:c.1582+161A=	ENSP00000483243.1:n.1582+161A=
NM_000769.2:c.819+161A=	NP_000760.1:n.819+161A=
NM_000769.4:c.819+161A= MANE Select	NP_000760.1:n.819+161A=