Canonical Allele Identifier: CA2336260381
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012471T= , CM000681.2:g.41012471T= GRCh38
NC_000019.9:g.41518376T= , CM000681.1:g.41518376T= GRCh37
NC_000019.8:g.46210216T= NCBI36
NG_007929.1:g.26173T=

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.1138T= MANE Select ENSP00000324648.2:p.Tyr380=
ENST00000598834.2:c.1162T=
ENST00000324071.8:c.1138T= ENSP00000324648.2:p.Tyr380=
ENST00000593831.1:c.430T= ENSP00000470582.1:p.Tyr144=
ENST00000597612.1:n.633T=
NM_000767.4:c.1138T= NP_000758.1:p.Tyr380=
XM_005258569.3:c.1138T= XP_005258626.1:p.Tyr380=
XM_006723050.2:c.1138T= XP_006723113.1:p.Tyr380=
XM_011526546.1:c.1138T= XP_011524848.1:p.Tyr380=
XM_011526547.1:c.1138T= XP_011524849.1:p.Tyr380=
XM_011526548.1:c.658T= XP_011524850.1:p.Tyr220=
XM_011526549.1:c.547T= XP_011524851.1:p.Tyr183=
XM_011526550.1:c.538T= XP_011524852.1:p.Tyr180=
NM_000767.5:c.1138T= MANE Select NP_000758.1:p.Tyr380=