Canonical Allele Identifier: CA2336260611

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012879_41012883delinsAAAAC , CM000681.2:g.41012879_41012883delinsAAAAC	GRCh38
NC_000019.9:g.41518784_41518788delinsAAAAC , CM000681.1:g.41518784_41518788delinsAAAAC	GRCh37
NC_000019.8:g.46210624_46210628delinsAAAAC	NCBI36
NG_007929.1:g.26581_26585delinsAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+64_1294+68delinsAAAAC MANE Select	ENSP00000324648.2:n.1294+64_1294+68delinsAAAAC
ENST00000598834.2:c.1177-94_1177-90delinsAAAAC
ENST00000324071.8:c.1294+64_1294+68delinsAAAAC	ENSP00000324648.2:n.1294+64_1294+68delinsAAAAC
ENST00000593831.1:c.586+64_586+68delinsAAAAC	ENSP00000470582.1:n.586+64_586+68delinsAAAAC
ENST00000597612.1:n.647+394_647+398delinsAAAAC
NM_000767.4:c.1294+64_1294+68delinsAAAAC	NP_000758.1:n.1294+64_1294+68delinsAAAAC
XM_005258569.3:c.1152+394_1152+398delinsAAAAC	XP_005258626.1:n.1152+394_1152+398delinsAAAAC
XM_006723050.2:c.1294+64_1294+68delinsAAAAC	XP_006723113.1:n.1294+64_1294+68delinsAAAAC
XM_011526546.1:c.1216_1220delinsAAAAC	XP_011524848.1:p.Lys406=
XM_011526547.1:c.1153-94_1153-90delinsAAAAC	XP_011524849.1:n.1153-94_1153-90delinsAAAAC
XM_011526548.1:c.814+64_814+68delinsAAAAC	XP_011524850.1:n.814+64_814+68delinsAAAAC
XM_011526549.1:c.703+64_703+68delinsAAAAC	XP_011524851.1:n.703+64_703+68delinsAAAAC
XM_011526550.1:c.694+64_694+68delinsAAAAC	XP_011524852.1:n.694+64_694+68delinsAAAAC
NM_000767.5:c.1294+64_1294+68delinsAAAAC MANE Select	NP_000758.1:n.1294+64_1294+68delinsAAAAC