Canonical Allele Identifier: CA2336260366

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012447A= , CM000681.2:g.41012447A=	GRCh38
NC_000019.9:g.41518352A= , CM000681.1:g.41518352A=	GRCh37
NC_000019.8:g.46210192A=	NCBI36
NG_007929.1:g.26149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1114A= MANE Select	ENSP00000324648.2:p.Thr372=
ENST00000598834.2:c.1138A=
ENST00000324071.8:c.1114A=	ENSP00000324648.2:p.Thr372=
ENST00000593831.1:c.406A=	ENSP00000470582.1:p.Thr136=
ENST00000597612.1:n.609A=
NM_000767.4:c.1114A=	NP_000758.1:p.Thr372=
XM_005258569.3:c.1114A=	XP_005258626.1:p.Thr372=
XM_006723050.2:c.1114A=	XP_006723113.1:p.Thr372=
XM_011526546.1:c.1114A=	XP_011524848.1:p.Thr372=
XM_011526547.1:c.1114A=	XP_011524849.1:p.Thr372=
XM_011526548.1:c.634A=	XP_011524850.1:p.Thr212=
XM_011526549.1:c.523A=	XP_011524851.1:p.Thr175=
XM_011526550.1:c.514A=	XP_011524852.1:p.Thr172=
NM_000767.5:c.1114A= MANE Select	NP_000758.1:p.Thr372=