Canonical Allele Identifier: CA2336260368

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012452A= , CM000681.2:g.41012452A=	GRCh38
NC_000019.9:g.41518357A= , CM000681.1:g.41518357A=	GRCh37
NC_000019.8:g.46210197A=	NCBI36
NG_007929.1:g.26154A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1119A= MANE Select	ENSP00000324648.2:p.Gln373=
ENST00000598834.2:c.1143A=
ENST00000324071.8:c.1119A=	ENSP00000324648.2:p.Gln373=
ENST00000593831.1:c.411A=	ENSP00000470582.1:p.Gln137=
ENST00000597612.1:n.614A=
NM_000767.4:c.1119A=	NP_000758.1:p.Gln373=
XM_005258569.3:c.1119A=	XP_005258626.1:p.Gln373=
XM_006723050.2:c.1119A=	XP_006723113.1:p.Gln373=
XM_011526546.1:c.1119A=	XP_011524848.1:p.Gln373=
XM_011526547.1:c.1119A=	XP_011524849.1:p.Gln373=
XM_011526548.1:c.639A=	XP_011524850.1:p.Gln213=
XM_011526549.1:c.528A=	XP_011524851.1:p.Gln176=
XM_011526550.1:c.519A=	XP_011524852.1:p.Gln173=
NM_000767.5:c.1119A= MANE Select	NP_000758.1:p.Gln373=