Canonical Allele Identifier: CA2336260325

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012369_41012370delinsAT , CM000681.2:g.41012369_41012370delinsAT	GRCh38
NC_000019.9:g.41518274_41518275delinsAT , CM000681.1:g.41518274_41518275delinsAT	GRCh37
NC_000019.8:g.46210114_46210115delinsAT	NCBI36
NG_007929.1:g.26071_26072delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1036_1037delinsAT MANE Select	ENSP00000324648.2:p.Met346=
ENST00000598834.2:c.1060_1061delinsAT
ENST00000324071.8:c.1036_1037delinsAT	ENSP00000324648.2:p.Met346=
ENST00000593831.1:c.328_329delinsAT	ENSP00000470582.1:p.Met110=
ENST00000597612.1:n.531_532delinsAT
NM_000767.4:c.1036_1037delinsAT	NP_000758.1:p.Met346=
XM_005258569.3:c.1036_1037delinsAT	XP_005258626.1:p.Met346=
XM_006723050.2:c.1036_1037delinsAT	XP_006723113.1:p.Met346=
XM_011526546.1:c.1036_1037delinsAT	XP_011524848.1:p.Met346=
XM_011526547.1:c.1036_1037delinsAT	XP_011524849.1:p.Met346=
XM_011526548.1:c.556_557delinsAT	XP_011524850.1:p.Met186=
XM_011526549.1:c.445_446delinsAT	XP_011524851.1:p.Met149=
XM_011526550.1:c.436_437delinsAT	XP_011524852.1:p.Met146=
NM_000767.5:c.1036_1037delinsAT MANE Select	NP_000758.1:p.Met346=