Canonical Allele Identifier: CA2336257532

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41007057T= , CM000681.2:g.41007057T=	GRCh38
NC_000019.9:g.41512962T= , CM000681.1:g.41512962T=	GRCh37
NC_000019.8:g.46204802T=	NCBI36
NG_007929.1:g.20759T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000767.5:c.637T= MANE Select	NP_000758.1:p.Phe213=
ENST00000324071.10:c.637T= MANE Select	ENSP00000324648.2:p.Phe213=
NM_000767.4:c.637T=	NP_000758.1:p.Phe213=
ENST00000324071.8:c.637T=	ENSP00000324648.2:p.Phe213=
ENST00000593831.1:c.256+2611T=	ENSP00000470582.1:n.256+2611T=
ENST00000594187.1:n.221T=
ENST00000598834.1:n.539T=
ENST00000598834.2:c.539T=
XM_005258569.3:c.637T=	XP_005258626.1:p.Phe213=
XM_006723050.2:c.637T=	XP_006723113.1:p.Phe213=
XM_011526546.1:c.637T=	XP_011524848.1:p.Phe213=
XM_011526547.1:c.637T=	XP_011524849.1:p.Phe213=
XM_011526548.1:c.484+2611T=	XP_011524850.1:n.484+2611T=
XM_011526549.1:c.46T=	XP_011524851.1:p.Phe16=
XM_011526550.1:c.364+2611T=	XP_011524852.1:n.364+2611T=