Canonical Allele Identifier: CA2336260372

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012459A= , CM000681.2:g.41012459A=	GRCh38
NC_000019.9:g.41518364A= , CM000681.1:g.41518364A=	GRCh37
NC_000019.8:g.46210204A=	NCBI36
NG_007929.1:g.26161A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1126A= MANE Select	ENSP00000324648.2:p.Ser376=
ENST00000598834.2:c.1150A=
ENST00000324071.8:c.1126A=	ENSP00000324648.2:p.Ser376=
ENST00000593831.1:c.418A=	ENSP00000470582.1:p.Ser140=
ENST00000597612.1:n.621A=
NM_000767.4:c.1126A=	NP_000758.1:p.Ser376=
XM_005258569.3:c.1126A=	XP_005258626.1:p.Ser376=
XM_006723050.2:c.1126A=	XP_006723113.1:p.Ser376=
XM_011526546.1:c.1126A=	XP_011524848.1:p.Ser376=
XM_011526547.1:c.1126A=	XP_011524849.1:p.Ser376=
XM_011526548.1:c.646A=	XP_011524850.1:p.Ser216=
XM_011526549.1:c.535A=	XP_011524851.1:p.Ser179=
XM_011526550.1:c.526A=	XP_011524852.1:p.Ser176=
NM_000767.5:c.1126A= MANE Select	NP_000758.1:p.Ser376=