Canonical Allele Identifier: CA2336256106
Community Standard Title: NM_000767.5(CYP2B6):c.415A= (p.Lys139=)
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41004377A= , CM000681.2:g.41004377A= GRCh38
NC_000019.9:g.41510282A= , CM000681.1:g.41510282A= GRCh37
NC_000019.8:g.46202122A= NCBI36
NG_007929.1:g.18079A=

Transcript Alleles

HGVS Amino-acid Change
NM_000767.5:c.415A= MANE Select NP_000758.1:p.Lys139=
ENST00000324071.10:c.415A= MANE Select ENSP00000324648.2:p.Lys139=
NM_000767.4:c.415A= NP_000758.1:p.Lys139=
ENST00000324071.8:c.415A= ENSP00000324648.2:p.Lys139=
ENST00000593831.1:c.187A= ENSP00000470582.1:p.Lys63=
ENST00000598834.1:n.317A=
ENST00000598834.2:c.317A=
XM_005258569.3:c.415A= XP_005258626.1:p.Lys139=
XM_006723050.2:c.415A= XP_006723113.1:p.Lys139=
XM_011526546.1:c.415A= XP_011524848.1:p.Lys139=
XM_011526547.1:c.415A= XP_011524849.1:p.Lys139=
XM_011526548.1:c.415A= XP_011524850.1:p.Lys139=
XM_011526549.1:c.-145A= XP_011524851.1:n.-145A=
XM_011526550.1:c.295A= XP_011524852.1:p.Lys99=