Canonical Allele Identifier: CA2842366318

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012389dup , CM000681.2:g.41012389dup	GRCh38
NC_000019.9:g.41518294dup , CM000681.1:g.41518294dup	GRCh37
NC_000019.8:g.46210134dup	NCBI36
NG_007929.1:g.26091dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1056dup MANE Select	ENSP00000324648.2:p.Ile353HisfsTer3
ENST00000598834.2:c.1080dup
ENST00000324071.8:c.1056dup	ENSP00000324648.2:p.Ile353HisfsTer3
ENST00000593831.1:c.348dup	ENSP00000470582.1:p.Ile117HisfsTer3
ENST00000597612.1:n.551dup
NM_000767.4:c.1056dup	NP_000758.1:p.Ile353HisfsTer3
XM_005258569.3:c.1056dup	XP_005258626.1:p.Ile353HisfsTer3
XM_006723050.2:c.1056dup	XP_006723113.1:p.Ile353HisfsTer3
XM_011526546.1:c.1056dup	XP_011524848.1:p.Ile353HisfsTer3
XM_011526547.1:c.1056dup	XP_011524849.1:p.Ile353HisfsTer3
XM_011526548.1:c.576dup	XP_011524850.1:p.Ile193HisfsTer3
XM_011526549.1:c.465dup	XP_011524851.1:p.Ile156HisfsTer3
XM_011526550.1:c.456dup	XP_011524852.1:p.Ile153HisfsTer3
NM_000767.5:c.1056dup MANE Select	NP_000758.1:p.Ile353HisfsTer3