Canonical Allele Identifier: CA405984686
Gene: CYP2B6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012439A>T , CM000681.2:g.41012439A>T GRCh38
NC_000019.9:g.41518344A>T , CM000681.1:g.41518344A>T GRCh37
NC_000019.8:g.46210184A>T NCBI36
NG_007929.1:g.26141A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1106A>T MANE Select ENSP00000324648.2:p.His369Leu
ENST00000598834.2:c.1130A>T
ENST00000324071.8:c.1106A>T ENSP00000324648.2:p.His369Leu
ENST00000593831.1:c.398A>T ENSP00000470582.1:p.His133Leu
ENST00000597612.1:n.601A>T
NM_000767.4:c.1106A>T NP_000758.1:p.His369Leu
XM_005258569.3:c.1106A>T XP_005258626.1:p.His369Leu
XM_006723050.2:c.1106A>T XP_006723113.1:p.His369Leu
XM_011526546.1:c.1106A>T XP_011524848.1:p.His369Leu
XM_011526547.1:c.1106A>T XP_011524849.1:p.His369Leu
XM_011526548.1:c.626A>T XP_011524850.1:p.His209Leu
XM_011526549.1:c.515A>T XP_011524851.1:p.His172Leu
XM_011526550.1:c.506A>T XP_011524852.1:p.His169Leu
NM_000767.5:c.1106A>T MANE Select NP_000758.1:p.His369Leu