Canonical Allele Identifier: CA2336260385
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012477A= , CM000681.2:g.41012477A= GRCh38
NC_000019.9:g.41518382A= , CM000681.1:g.41518382A= GRCh37
NC_000019.8:g.46210222A= NCBI36
NG_007929.1:g.26179A=

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.1144A= MANE Select ENSP00000324648.2:p.Ile382=
ENST00000598834.2:c.1168A=
ENST00000324071.8:c.1144A= ENSP00000324648.2:p.Ile382=
ENST00000593831.1:c.436A= ENSP00000470582.1:p.Ile146=
ENST00000597612.1:n.639A=
NM_000767.4:c.1144A= NP_000758.1:p.Ile382=
XM_005258569.3:c.1144A= XP_005258626.1:p.Ile382=
XM_006723050.2:c.1144A= XP_006723113.1:p.Ile382=
XM_011526546.1:c.1144A= XP_011524848.1:p.Ile382=
XM_011526547.1:c.1144A= XP_011524849.1:p.Ile382=
XM_011526548.1:c.664A= XP_011524850.1:p.Ile222=
XM_011526549.1:c.553A= XP_011524851.1:p.Ile185=
XM_011526550.1:c.544A= XP_011524852.1:p.Ile182=
NM_000767.5:c.1144A= MANE Select NP_000758.1:p.Ile382=