Canonical Allele Identifier: CA2336260530

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012705C= , CM000681.2:g.41012705C=	GRCh38
NC_000019.9:g.41518610C= , CM000681.1:g.41518610C=	GRCh37
NC_000019.8:g.46210450C=	NCBI36
NG_007929.1:g.26407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1184C= MANE Select	ENSP00000324648.2:p.Ala395=
ENST00000598834.2:c.1176+220C=
ENST00000324071.8:c.1184C=	ENSP00000324648.2:p.Ala395=
ENST00000593831.1:c.476C=	ENSP00000470582.1:p.Ala159=
ENST00000597612.1:n.647+220C=
NM_000767.4:c.1184C=	NP_000758.1:p.Ala395=
XM_005258569.3:c.1152+220C=	XP_005258626.1:n.1152+220C=
XM_006723050.2:c.1184C=	XP_006723113.1:p.Ala395=
XM_011526546.1:c.1153-111C=	XP_011524848.1:n.1153-111C=
XM_011526547.1:c.1152+220C=	XP_011524849.1:n.1152+220C=
XM_011526548.1:c.704C=	XP_011524850.1:p.Ala235=
XM_011526549.1:c.593C=	XP_011524851.1:p.Ala198=
XM_011526550.1:c.584C=	XP_011524852.1:p.Ala195=
NM_000767.5:c.1184C= MANE Select	NP_000758.1:p.Ala395=