Canonical Allele Identifier: CA2336260570

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012799T= , CM000681.2:g.41012799T=	GRCh38
NC_000019.9:g.41518704T= , CM000681.1:g.41518704T=	GRCh37
NC_000019.8:g.46210544T=	NCBI36
NG_007929.1:g.26501T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1278T= MANE Select	ENSP00000324648.2:p.Phe426=
ENST00000598834.2:c.1177-174T=
ENST00000324071.8:c.1278T=	ENSP00000324648.2:p.Phe426=
ENST00000593831.1:c.570T=	ENSP00000470582.1:p.Phe190=
ENST00000597612.1:n.647+314T=
NM_000767.4:c.1278T=	NP_000758.1:p.Phe426=
XM_005258569.3:c.1152+314T=	XP_005258626.1:n.1152+314T=
XM_006723050.2:c.1278T=	XP_006723113.1:p.Phe426=
XM_011526546.1:c.1153-17T=	XP_011524848.1:n.1153-17T=
XM_011526547.1:c.1153-174T=	XP_011524849.1:n.1153-174T=
XM_011526548.1:c.798T=	XP_011524850.1:p.Phe266=
XM_011526549.1:c.687T=	XP_011524851.1:p.Phe229=
XM_011526550.1:c.678T=	XP_011524852.1:p.Phe226=
NM_000767.5:c.1278T= MANE Select	NP_000758.1:p.Phe426=