Canonical Allele Identifier: CA2336260346
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012416C= , CM000681.2:g.41012416C= GRCh38
NC_000019.9:g.41518321C= , CM000681.1:g.41518321C= GRCh37
NC_000019.8:g.46210161C= NCBI36
NG_007929.1:g.26118C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1083C= MANE Select ENSP00000324648.2:p.Asp361=
ENST00000598834.2:c.1107C=
ENST00000324071.8:c.1083C= ENSP00000324648.2:p.Asp361=
ENST00000593831.1:c.375C= ENSP00000470582.1:p.Asp125=
ENST00000597612.1:n.578C=
NM_000767.4:c.1083C= NP_000758.1:p.Asp361=
XM_005258569.3:c.1083C= XP_005258626.1:p.Asp361=
XM_006723050.2:c.1083C= XP_006723113.1:p.Asp361=
XM_011526546.1:c.1083C= XP_011524848.1:p.Asp361=
XM_011526547.1:c.1083C= XP_011524849.1:p.Asp361=
XM_011526548.1:c.603C= XP_011524850.1:p.Asp201=
XM_011526549.1:c.492C= XP_011524851.1:p.Asp164=
XM_011526550.1:c.483C= XP_011524852.1:p.Asp161=
NM_000767.5:c.1083C= MANE Select NP_000758.1:p.Asp361=