Canonical Allele Identifier: CA2576790770

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012842C>A , CM000681.2:g.41012842C>A	GRCh38
NC_000019.9:g.41518747C>A , CM000681.1:g.41518747C>A	GRCh37
NC_000019.8:g.46210587C>A	NCBI36
NG_007929.1:g.26544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+27C>A MANE Select	ENSP00000324648.2:n.1294+27C>A
ENST00000598834.2:c.1177-131C>A
ENST00000324071.8:c.1294+27C>A	ENSP00000324648.2:n.1294+27C>A
ENST00000593831.1:c.586+27C>A	ENSP00000470582.1:n.586+27C>A
ENST00000597612.1:n.647+357C>A
NM_000767.4:c.1294+27C>A	NP_000758.1:n.1294+27C>A
XM_005258569.3:c.1152+357C>A	XP_005258626.1:n.1152+357C>A
XM_006723050.2:c.1294+27C>A	XP_006723113.1:n.1294+27C>A
XM_011526546.1:c.1179C>A	XP_011524848.1:p.Pro393=
XM_011526547.1:c.1153-131C>A	XP_011524849.1:n.1153-131C>A
XM_011526548.1:c.814+27C>A	XP_011524850.1:n.814+27C>A
XM_011526549.1:c.703+27C>A	XP_011524851.1:n.703+27C>A
XM_011526550.1:c.694+27C>A	XP_011524852.1:n.694+27C>A
NM_000767.5:c.1294+27C>A MANE Select	NP_000758.1:n.1294+27C>A