Canonical Allele Identifier: CA2336256052

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41004277A= , CM000681.2:g.41004277A=	GRCh38
NC_000019.9:g.41510182A= , CM000681.1:g.41510182A=	GRCh37
NC_000019.8:g.46202022A=	NCBI36
NG_007929.1:g.17979A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.335-20A= MANE Select	ENSP00000324648.2:n.335-20A=
ENST00000598834.2:c.237-20A=
ENST00000324071.8:c.335-20A=	ENSP00000324648.2:n.335-20A=
ENST00000593831.1:c.107-20A=	ENSP00000470582.1:n.107-20A=
ENST00000598834.1:n.237-20A=
NM_000767.4:c.335-20A=	NP_000758.1:n.335-20A=
XM_005258569.3:c.335-20A=	XP_005258626.1:n.335-20A=
XM_006723050.2:c.335-20A=	XP_006723113.1:n.335-20A=
XM_011526546.1:c.335-20A=	XP_011524848.1:n.335-20A=
XM_011526547.1:c.335-20A=	XP_011524849.1:n.335-20A=
XM_011526548.1:c.335-20A=	XP_011524850.1:n.335-20A=
XM_011526550.1:c.215-20A=	XP_011524852.1:n.215-20A=
NM_000767.5:c.335-20A= MANE Select	NP_000758.1:n.335-20A=