Canonical Allele Identifier: CA2336258617

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41009268G= , CM000681.2:g.41009268G=	GRCh38
NC_000019.9:g.41515173G= , CM000681.1:g.41515173G=	GRCh37
NC_000019.8:g.46207013G=	NCBI36
NG_007929.1:g.22970G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.695G= MANE Select	ENSP00000324648.2:p.Arg232=
ENST00000598834.2:c.719G=
ENST00000324071.8:c.695G=	ENSP00000324648.2:p.Arg232=
ENST00000593831.1:c.257-3030G=	ENSP00000470582.1:n.257-3030G=
NM_000767.4:c.695G=	NP_000758.1:p.Arg232=
XM_005258569.3:c.695G=	XP_005258626.1:p.Arg232=
XM_006723050.2:c.695G=	XP_006723113.1:p.Arg232=
XM_011526546.1:c.695G=	XP_011524848.1:p.Arg232=
XM_011526547.1:c.695G=	XP_011524849.1:p.Arg232=
XM_011526548.1:c.485-3030G=	XP_011524850.1:n.485-3030G=
XM_011526549.1:c.104G=	XP_011524851.1:p.Arg35=
XM_011526550.1:c.365-3030G=	XP_011524852.1:n.365-3030G=
NM_000767.5:c.695G= MANE Select	NP_000758.1:p.Arg232=