Canonical Allele Identifier: CA2336260576

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012807_41012810delinsTCTC , CM000681.2:g.41012807_41012810delinsTCTC	GRCh38
NC_000019.9:g.41518712_41518715delinsTCTC , CM000681.1:g.41518712_41518715delinsTCTC	GRCh37
NC_000019.8:g.46210552_46210555delinsTCTC	NCBI36
NG_007929.1:g.26509_26512delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1286_1289delinsTCTC MANE Select	ENSP00000324648.2:p.Phe429=
ENST00000598834.2:c.1177-166_1177-163delinsTCTC
ENST00000324071.8:c.1286_1289delinsTCTC	ENSP00000324648.2:p.Phe429=
ENST00000593831.1:c.578_581delinsTCTC	ENSP00000470582.1:p.Phe193=
ENST00000597612.1:n.647+322_647+325delinsTCTC
NM_000767.4:c.1286_1289delinsTCTC	NP_000758.1:p.Phe429=
XM_005258569.3:c.1152+322_1152+325delinsTCTC	XP_005258626.1:n.1152+322_1152+325delinsTCTC
XM_006723050.2:c.1286_1289delinsTCTC	XP_006723113.1:p.Phe429=
XM_011526546.1:c.1153-9_1153-6delinsTCTC	XP_011524848.1:n.1153-9_1153-6delinsTCTC
XM_011526547.1:c.1153-166_1153-163delinsTCTC	XP_011524849.1:n.1153-166_1153-163delinsTCTC
XM_011526548.1:c.806_809delinsTCTC	XP_011524850.1:p.Phe269=
XM_011526549.1:c.695_698delinsTCTC	XP_011524851.1:p.Phe232=
XM_011526550.1:c.686_689delinsTCTC	XP_011524852.1:p.Phe229=
NM_000767.5:c.1286_1289delinsTCTC MANE Select	NP_000758.1:p.Phe429=