Canonical Allele Identifier: CA2576790622

Gene: CYP2B6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41006814A>T , CM000681.2:g.41006814A>T	GRCh38
NC_000019.9:g.41512719A>T , CM000681.1:g.41512719A>T	GRCh37
NC_000019.8:g.46204559A>T	NCBI36
NG_007929.1:g.20516A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.485-91A>T MANE Select	ENSP00000324648.2:n.485-91A>T
ENST00000598834.2:c.387-91A>T
ENST00000324071.8:c.485-91A>T	ENSP00000324648.2:n.485-91A>T
ENST00000593831.1:c.256+2368A>T	ENSP00000470582.1:n.256+2368A>T
ENST00000594187.1:n.69-91A>T
ENST00000598834.1:n.387-91A>T
NM_000767.4:c.485-91A>T	NP_000758.1:n.485-91A>T
XM_005258569.3:c.485-91A>T	XP_005258626.1:n.485-91A>T
XM_006723050.2:c.485-91A>T	XP_006723113.1:n.485-91A>T
XM_011526546.1:c.485-91A>T	XP_011524848.1:n.485-91A>T
XM_011526547.1:c.485-91A>T	XP_011524849.1:n.485-91A>T
XM_011526548.1:c.484+2368A>T	XP_011524850.1:n.484+2368A>T
XM_011526549.1:c.-75-123A>T	XP_011524851.1:n.-75-123A>T
XM_011526550.1:c.364+2368A>T	XP_011524852.1:n.364+2368A>T
NM_000767.5:c.485-91A>T MANE Select	NP_000758.1:n.485-91A>T