Canonical Allele Identifier: CA2336260572

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012802C= , CM000681.2:g.41012802C=	GRCh38
NC_000019.9:g.41518707C= , CM000681.1:g.41518707C=	GRCh37
NC_000019.8:g.46210547C=	NCBI36
NG_007929.1:g.26504C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1281C= MANE Select	ENSP00000324648.2:p.Ile427=
ENST00000598834.2:c.1177-171C=
ENST00000324071.8:c.1281C=	ENSP00000324648.2:p.Ile427=
ENST00000593831.1:c.573C=	ENSP00000470582.1:p.Ile191=
ENST00000597612.1:n.647+317C=
NM_000767.4:c.1281C=	NP_000758.1:p.Ile427=
XM_005258569.3:c.1152+317C=	XP_005258626.1:n.1152+317C=
XM_006723050.2:c.1281C=	XP_006723113.1:p.Ile427=
XM_011526546.1:c.1153-14C=	XP_011524848.1:n.1153-14C=
XM_011526547.1:c.1153-171C=	XP_011524849.1:n.1153-171C=
XM_011526548.1:c.801C=	XP_011524850.1:p.Ile267=
XM_011526549.1:c.690C=	XP_011524851.1:p.Ile230=
XM_011526550.1:c.681C=	XP_011524852.1:p.Ile227=
NM_000767.5:c.1281C= MANE Select	NP_000758.1:p.Ile427=