Canonical Allele Identifier: CA2336255672

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41003533T= , CM000681.2:g.41003533T=	GRCh38
NC_000019.9:g.41509438T= , CM000681.1:g.41509438T=	GRCh37
NC_000019.8:g.46201278T=	NCBI36
NG_007929.1:g.17235T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000767.5:c.172-468T= MANE Select	NP_000758.1:n.172-468T=
ENST00000324071.10:c.172-468T= MANE Select	ENSP00000324648.2:n.172-468T=
NM_000767.4:c.172-468T=	NP_000758.1:n.172-468T=
ENST00000324071.8:c.172-468T=	ENSP00000324648.2:n.172-468T=
ENST00000598834.1:n.74-468T=
ENST00000598834.2:c.74-468T=
XM_005258569.3:c.172-468T=	XP_005258626.1:n.172-468T=
XM_006723050.2:c.172-468T=	XP_006723113.1:n.172-468T=
XM_011526546.1:c.172-468T=	XP_011524848.1:n.172-468T=
XM_011526547.1:c.172-468T=	XP_011524849.1:n.172-468T=
XM_011526548.1:c.172-468T=	XP_011524850.1:n.172-468T=