Canonical Allele Identifier: CA2336260522

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012683G= , CM000681.2:g.41012683G=	GRCh38
NC_000019.9:g.41518588G= , CM000681.1:g.41518588G=	GRCh37
NC_000019.8:g.46210428G=	NCBI36
NG_007929.1:g.26385G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1162G= MANE Select	ENSP00000324648.2:p.Val388=
ENST00000598834.2:c.1176+198G=
ENST00000324071.8:c.1162G=	ENSP00000324648.2:p.Val388=
ENST00000593831.1:c.454G=	ENSP00000470582.1:p.Val152=
ENST00000597612.1:n.647+198G=
NM_000767.4:c.1162G=	NP_000758.1:p.Val388=
XM_005258569.3:c.1152+198G=	XP_005258626.1:n.1152+198G=
XM_006723050.2:c.1162G=	XP_006723113.1:p.Val388=
XM_011526546.1:c.1153-133G=	XP_011524848.1:n.1153-133G=
XM_011526547.1:c.1152+198G=	XP_011524849.1:n.1152+198G=
XM_011526548.1:c.682G=	XP_011524850.1:p.Val228=
XM_011526549.1:c.571G=	XP_011524851.1:p.Val191=
XM_011526550.1:c.562G=	XP_011524852.1:p.Val188=
NM_000767.5:c.1162G= MANE Select	NP_000758.1:p.Val388=