Canonical Allele Identifier: CA9455475
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs776037494

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012423C>A , CM000681.2:g.41012423C>A GRCh38
NC_000019.9:g.41518328C>A , CM000681.1:g.41518328C>A GRCh37
NC_000019.8:g.46210168C>A NCBI36
NG_007929.1:g.26125C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1090C>A MANE Select ENSP00000324648.2:p.Pro364Thr
ENST00000598834.2:c.1114C>A
ENST00000324071.8:c.1090C>A ENSP00000324648.2:p.Pro364Thr
ENST00000593831.1:c.382C>A ENSP00000470582.1:p.Pro128Thr
ENST00000597612.1:n.585C>A
NM_000767.4:c.1090C>A NP_000758.1:p.Pro364Thr
XM_005258569.3:c.1090C>A XP_005258626.1:p.Pro364Thr
XM_006723050.2:c.1090C>A XP_006723113.1:p.Pro364Thr
XM_011526546.1:c.1090C>A XP_011524848.1:p.Pro364Thr
XM_011526547.1:c.1090C>A XP_011524849.1:p.Pro364Thr
XM_011526548.1:c.610C>A XP_011524850.1:p.Pro204Thr
XM_011526549.1:c.499C>A XP_011524851.1:p.Pro167Thr
XM_011526550.1:c.490C>A XP_011524852.1:p.Pro164Thr
NM_000767.5:c.1090C>A MANE Select NP_000758.1:p.Pro364Thr