Canonical Allele Identifier: CA2336260446

Gene: CYP2B6

Linked Data

• dbSNP Id: rs1969302262

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012577_41012586del , CM000681.2:g.41012577_41012586del	GRCh38
NC_000019.9:g.41518482_41518491del , CM000681.1:g.41518482_41518491del	GRCh37
NC_000019.8:g.46210322_46210331del	NCBI36
NG_007929.1:g.26279_26288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1152+92_1153-88del MANE Select	ENSP00000324648.2:n.1152+92_1153-88del
ENST00000598834.2:c.1176+92_1176+101del
ENST00000324071.8:c.1152+92_1153-88del	ENSP00000324648.2:n.1152+92_1153-88del
ENST00000593831.1:c.444+92_445-88del	ENSP00000470582.1:n.444+92_445-88del
ENST00000597612.1:n.647+92_647+101del
NM_000767.4:c.1152+92_1153-88del	NP_000758.1:n.1152+92_1153-88del
XM_005258569.3:c.1152+92_1152+101del	XP_005258626.1:n.1152+92_1152+101del
XM_006723050.2:c.1152+92_1153-88del	XP_006723113.1:n.1152+92_1153-88del
XM_011526546.1:c.1152+92_1152+101del	XP_011524848.1:n.1152+92_1152+101del
XM_011526547.1:c.1152+92_1152+101del	XP_011524849.1:n.1152+92_1152+101del
XM_011526548.1:c.672+92_673-88del	XP_011524850.1:n.672+92_673-88del
XM_011526549.1:c.561+92_562-88del	XP_011524851.1:n.561+92_562-88del
XM_011526550.1:c.552+92_553-88del	XP_011524852.1:n.552+92_553-88del
NM_000767.5:c.1152+92_1153-88del MANE Select	NP_000758.1:n.1152+92_1153-88del