Canonical Allele Identifier: CA2336260343
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012413C= , CM000681.2:g.41012413C= GRCh38
NC_000019.9:g.41518318C= , CM000681.1:g.41518318C= GRCh37
NC_000019.8:g.46210158C= NCBI36
NG_007929.1:g.26115C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1080C= MANE Select ENSP00000324648.2:p.Ser360=
ENST00000598834.2:c.1104C=
ENST00000324071.8:c.1080C= ENSP00000324648.2:p.Ser360=
ENST00000593831.1:c.372C= ENSP00000470582.1:p.Ser124=
ENST00000597612.1:n.575C=
NM_000767.4:c.1080C= NP_000758.1:p.Ser360=
XM_005258569.3:c.1080C= XP_005258626.1:p.Ser360=
XM_006723050.2:c.1080C= XP_006723113.1:p.Ser360=
XM_011526546.1:c.1080C= XP_011524848.1:p.Ser360=
XM_011526547.1:c.1080C= XP_011524849.1:p.Ser360=
XM_011526548.1:c.600C= XP_011524850.1:p.Ser200=
XM_011526549.1:c.489C= XP_011524851.1:p.Ser163=
XM_011526550.1:c.480C= XP_011524852.1:p.Ser160=
NM_000767.5:c.1080C= MANE Select NP_000758.1:p.Ser360=