Canonical Allele Identifier: CA405980821
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1439397400

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41009378C>G , CM000681.2:g.41009378C>G GRCh38
NC_000019.9:g.41515283C>G , CM000681.1:g.41515283C>G GRCh37
NC_000019.8:g.46207123C>G NCBI36
NG_007929.1:g.23080C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.805C>G MANE Select ENSP00000324648.2:p.Leu269Val
ENST00000598834.2:c.829C>G
ENST00000324071.8:c.805C>G ENSP00000324648.2:p.Leu269Val
ENST00000593831.1:c.257-2920C>G ENSP00000470582.1:n.257-2920C>G
NM_000767.4:c.805C>G NP_000758.1:p.Leu269Val
XM_005258569.3:c.805C>G XP_005258626.1:p.Leu269Val
XM_006723050.2:c.805C>G XP_006723113.1:p.Leu269Val
XM_011526546.1:c.805C>G XP_011524848.1:p.Leu269Val
XM_011526547.1:c.805C>G XP_011524849.1:p.Leu269Val
XM_011526548.1:c.485-2920C>G XP_011524850.1:n.485-2920C>G
XM_011526549.1:c.214C>G XP_011524851.1:p.Leu72Val
XM_011526550.1:c.365-2920C>G XP_011524852.1:n.365-2920C>G
NM_000767.5:c.805C>G MANE Select NP_000758.1:p.Leu269Val