Canonical Allele Identifier: CA2336257499

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41006992A= , CM000681.2:g.41006992A=	GRCh38
NC_000019.9:g.41512897A= , CM000681.1:g.41512897A=	GRCh37
NC_000019.8:g.46204737A=	NCBI36
NG_007929.1:g.20694A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.572A= MANE Select	ENSP00000324648.2:p.Gln191=
ENST00000598834.2:c.474A=
ENST00000324071.8:c.572A=	ENSP00000324648.2:p.Gln191=
ENST00000593831.1:c.256+2546A=	ENSP00000470582.1:n.256+2546A=
ENST00000594187.1:n.156A=
ENST00000598834.1:n.474A=
NM_000767.4:c.572A=	NP_000758.1:p.Gln191=
XM_005258569.3:c.572A=	XP_005258626.1:p.Gln191=
XM_006723050.2:c.572A=	XP_006723113.1:p.Gln191=
XM_011526546.1:c.572A=	XP_011524848.1:p.Gln191=
XM_011526547.1:c.572A=	XP_011524849.1:p.Gln191=
XM_011526548.1:c.484+2546A=	XP_011524850.1:n.484+2546A=
XM_011526549.1:c.-20A=	XP_011524851.1:n.-20A=
XM_011526550.1:c.364+2546A=	XP_011524852.1:n.364+2546A=
NM_000767.5:c.572A= MANE Select	NP_000758.1:p.Gln191=