Canonical Allele Identifier: CA2511401651

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012700_41012701insG , CM000681.2:g.41012700_41012701insG	GRCh38
NC_000019.9:g.41518605_41518606insG , CM000681.1:g.41518605_41518606insG	GRCh37
NC_000019.8:g.46210445_46210446insG	NCBI36
NG_007929.1:g.26402_26403insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1179_1180insG MANE Select	ENSP00000324648.2:p.Thr394AspfsTer5
ENST00000598834.2:c.1176+215_1176+216insG
ENST00000324071.8:c.1179_1180insG	ENSP00000324648.2:p.Thr394AspfsTer5
ENST00000593831.1:c.471_472insG	ENSP00000470582.1:p.Thr158AspfsTer5
ENST00000597612.1:n.647+215_647+216insG
NM_000767.4:c.1179_1180insG	NP_000758.1:p.Thr394AspfsTer5
XM_005258569.3:c.1152+215_1152+216insG	XP_005258626.1:n.1152+215_1152+216insG
XM_006723050.2:c.1179_1180insG	XP_006723113.1:p.Thr394AspfsTer5
XM_011526546.1:c.1153-116_1153-115insG	XP_011524848.1:n.1153-116_1153-115insG
XM_011526547.1:c.1152+215_1152+216insG	XP_011524849.1:n.1152+215_1152+216insG
XM_011526548.1:c.699_700insG	XP_011524850.1:p.Thr234AspfsTer5
XM_011526549.1:c.588_589insG	XP_011524851.1:p.Thr197AspfsTer5
XM_011526550.1:c.579_580insG	XP_011524852.1:p.Thr194AspfsTer5
NM_000767.5:c.1179_1180insG MANE Select	NP_000758.1:p.Thr394AspfsTer5