Canonical Allele Identifier: CA2336260556

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012765A= , CM000681.2:g.41012765A=	GRCh38
NC_000019.9:g.41518670A= , CM000681.1:g.41518670A=	GRCh37
NC_000019.8:g.46210510A=	NCBI36
NG_007929.1:g.26467A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1244A= MANE Select	ENSP00000324648.2:p.Asp415=
ENST00000598834.2:c.1177-208A=
ENST00000324071.8:c.1244A=	ENSP00000324648.2:p.Asp415=
ENST00000593831.1:c.536A=	ENSP00000470582.1:p.Asp179=
ENST00000597612.1:n.647+280A=
NM_000767.4:c.1244A=	NP_000758.1:p.Asp415=
XM_005258569.3:c.1152+280A=	XP_005258626.1:n.1152+280A=
XM_006723050.2:c.1244A=	XP_006723113.1:p.Asp415=
XM_011526546.1:c.1153-51A=	XP_011524848.1:n.1153-51A=
XM_011526547.1:c.1153-208A=	XP_011524849.1:n.1153-208A=
XM_011526548.1:c.764A=	XP_011524850.1:p.Asp255=
XM_011526549.1:c.653A=	XP_011524851.1:p.Asp218=
XM_011526550.1:c.644A=	XP_011524852.1:p.Asp215=
NM_000767.5:c.1244A= MANE Select	NP_000758.1:p.Asp415=