Canonical Allele Identifier: CA2585217239

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012880-AAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012884_41012886del , CM000681.2:g.41012884_41012886del	GRCh38
NC_000019.9:g.41518789_41518791del , CM000681.1:g.41518789_41518791del	GRCh37
NC_000019.8:g.46210629_46210631del	NCBI36
NG_007929.1:g.26586_26588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+69_1294+71del MANE Select	ENSP00000324648.2:n.1294+69_1294+71del
ENST00000598834.2:c.1177-89_1177-87del
ENST00000324071.8:c.1294+69_1294+71del	ENSP00000324648.2:n.1294+69_1294+71del
ENST00000593831.1:c.586+69_586+71del	ENSP00000470582.1:n.586+69_586+71del
ENST00000597612.1:n.647+399_647+401del
NM_000767.4:c.1294+69_1294+71del	NP_000758.1:n.1294+69_1294+71del
XM_005258569.3:c.1152+399_1152+401del	XP_005258626.1:n.1152+399_1152+401del
XM_006723050.2:c.1294+69_1294+71del	XP_006723113.1:n.1294+69_1294+71del
XM_011526546.1:c.1221_1223del	XP_011524848.1:p.Thr408del
XM_011526547.1:c.1153-89_1153-87del	XP_011524849.1:n.1153-89_1153-87del
XM_011526548.1:c.814+69_814+71del	XP_011524850.1:n.814+69_814+71del
XM_011526549.1:c.703+69_703+71del	XP_011524851.1:n.703+69_703+71del
XM_011526550.1:c.694+69_694+71del	XP_011524852.1:n.694+69_694+71del
NM_000767.5:c.1294+69_1294+71del MANE Select	NP_000758.1:n.1294+69_1294+71del