Canonical Allele Identifier: CA2336260534

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012715C= , CM000681.2:g.41012715C=	GRCh38
NC_000019.9:g.41518620C= , CM000681.1:g.41518620C=	GRCh37
NC_000019.8:g.46210460C=	NCBI36
NG_007929.1:g.26417C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1194C= MANE Select	ENSP00000324648.2:p.Asp398=
ENST00000598834.2:c.1176+230C=
ENST00000324071.8:c.1194C=	ENSP00000324648.2:p.Asp398=
ENST00000593831.1:c.486C=	ENSP00000470582.1:p.Asp162=
ENST00000597612.1:n.647+230C=
NM_000767.4:c.1194C=	NP_000758.1:p.Asp398=
XM_005258569.3:c.1152+230C=	XP_005258626.1:n.1152+230C=
XM_006723050.2:c.1194C=	XP_006723113.1:p.Asp398=
XM_011526546.1:c.1153-101C=	XP_011524848.1:n.1153-101C=
XM_011526547.1:c.1152+230C=	XP_011524849.1:n.1152+230C=
XM_011526548.1:c.714C=	XP_011524850.1:p.Asp238=
XM_011526549.1:c.603C=	XP_011524851.1:p.Asp201=
XM_011526550.1:c.594C=	XP_011524852.1:p.Asp198=
NM_000767.5:c.1194C= MANE Select	NP_000758.1:p.Asp398=