Canonical Allele Identifier: CA2336260531
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012707C= , CM000681.2:g.41012707C= GRCh38
NC_000019.9:g.41518612C= , CM000681.1:g.41518612C= GRCh37
NC_000019.8:g.46210452C= NCBI36
NG_007929.1:g.26409C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1186C= MANE Select ENSP00000324648.2:p.Leu396=
ENST00000598834.2:c.1176+222C=
ENST00000324071.8:c.1186C= ENSP00000324648.2:p.Leu396=
ENST00000593831.1:c.478C= ENSP00000470582.1:p.Leu160=
ENST00000597612.1:n.647+222C=
NM_000767.4:c.1186C= NP_000758.1:p.Leu396=
XM_005258569.3:c.1152+222C= XP_005258626.1:n.1152+222C=
XM_006723050.2:c.1186C= XP_006723113.1:p.Leu396=
XM_011526546.1:c.1153-109C= XP_011524848.1:n.1153-109C=
XM_011526547.1:c.1152+222C= XP_011524849.1:n.1152+222C=
XM_011526548.1:c.706C= XP_011524850.1:p.Leu236=
XM_011526549.1:c.595C= XP_011524851.1:p.Leu199=
XM_011526550.1:c.586C= XP_011524852.1:p.Leu196=
NM_000767.5:c.1186C= MANE Select NP_000758.1:p.Leu396=