Canonical Allele Identifier: CA2336260297

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012319A= , CM000681.2:g.41012319A=	GRCh38
NC_000019.9:g.41518224A= , CM000681.1:g.41518224A=	GRCh37
NC_000019.8:g.46210064A=	NCBI36
NG_007929.1:g.26021A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.986A= MANE Select	ENSP00000324648.2:p.Glu329=
ENST00000598834.2:c.1010A=
ENST00000324071.8:c.986A=	ENSP00000324648.2:p.Glu329=
ENST00000593831.1:c.278A=	ENSP00000470582.1:p.Glu93=
ENST00000597612.1:n.481A=
NM_000767.4:c.986A=	NP_000758.1:p.Glu329=
XM_005258569.3:c.986A=	XP_005258626.1:p.Glu329=
XM_006723050.2:c.986A=	XP_006723113.1:p.Glu329=
XM_011526546.1:c.986A=	XP_011524848.1:p.Glu329=
XM_011526547.1:c.986A=	XP_011524849.1:p.Glu329=
XM_011526548.1:c.506A=	XP_011524850.1:p.Glu169=
XM_011526549.1:c.395A=	XP_011524851.1:p.Glu132=
XM_011526550.1:c.386A=	XP_011524852.1:p.Glu129=
NM_000767.5:c.986A= MANE Select	NP_000758.1:p.Glu329=