Canonical Allele Identifier: CA2336263272

Gene: CYP2B6

Linked Data

• dbSNP Id: rs1969396569

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41017987_41017988insCTT , CM000681.2:g.41017987_41017988insCTT	GRCh38
NC_000019.9:g.41523892_41523893insCTT , CM000681.1:g.41523892_41523893insCTT	GRCh37
NC_000019.8:g.46215732_46215733insCTT	NCBI36
NG_007929.1:g.31689_31690insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.*1160_*1161insCTT MANE Select	ENSP00000324648.2:n.*1160_*1161insCTT
ENST00000324071.8:c.*1160_*1161insCTT	ENSP00000324648.2:n.*1160_*1161insCTT
NM_000767.4:c.*1160_*1161insCTT	NP_000758.1:n.*1160_*1161insCTT
XM_011526548.1:c.*1160_*1161insCTT	XP_011524850.1:n.*1160_*1161insCTT
XM_011526549.1:c.*1160_*1161insCTT	XP_011524851.1:n.*1160_*1161insCTT
XM_011526550.1:c.*1160_*1161insCTT	XP_011524852.1:n.*1160_*1161insCTT
NM_000767.5:c.*1160_*1161insCTT MANE Select	NP_000758.1:n.*1160_*1161insCTT