Canonical Allele Identifier: CA2336260559

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012771A= , CM000681.2:g.41012771A=	GRCh38
NC_000019.9:g.41518676A= , CM000681.1:g.41518676A=	GRCh37
NC_000019.8:g.46210516A=	NCBI36
NG_007929.1:g.26473A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1250A= MANE Select	ENSP00000324648.2:p.Asn417=
ENST00000598834.2:c.1177-202A=
ENST00000324071.8:c.1250A=	ENSP00000324648.2:p.Asn417=
ENST00000593831.1:c.542A=	ENSP00000470582.1:p.Asn181=
ENST00000597612.1:n.647+286A=
NM_000767.4:c.1250A=	NP_000758.1:p.Asn417=
XM_005258569.3:c.1152+286A=	XP_005258626.1:n.1152+286A=
XM_006723050.2:c.1250A=	XP_006723113.1:p.Asn417=
XM_011526546.1:c.1153-45A=	XP_011524848.1:n.1153-45A=
XM_011526547.1:c.1153-202A=	XP_011524849.1:n.1153-202A=
XM_011526548.1:c.770A=	XP_011524850.1:p.Asn257=
XM_011526549.1:c.659A=	XP_011524851.1:p.Asn220=
XM_011526550.1:c.650A=	XP_011524852.1:p.Asn217=
NM_000767.5:c.1250A= MANE Select	NP_000758.1:p.Asn417=