Canonical Allele Identifier: CA2336263277
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1969396702

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41017990_41017991insG , CM000681.2:g.41017990_41017991insG GRCh38
NC_000019.9:g.41523895_41523896insG , CM000681.1:g.41523895_41523896insG GRCh37
NC_000019.8:g.46215735_46215736insG NCBI36
NG_007929.1:g.31692_31693insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1163_*1164insG MANE Select ENSP00000324648.2:n.*1163_*1164insG
ENST00000324071.8:c.*1163_*1164insG ENSP00000324648.2:n.*1163_*1164insG
NM_000767.4:c.*1163_*1164insG NP_000758.1:n.*1163_*1164insG
XM_011526548.1:c.*1163_*1164insG XP_011524850.1:n.*1163_*1164insG
XM_011526549.1:c.*1163_*1164insG XP_011524851.1:n.*1163_*1164insG
XM_011526550.1:c.*1163_*1164insG XP_011524852.1:n.*1163_*1164insG
NM_000767.5:c.*1163_*1164insG MANE Select NP_000758.1:n.*1163_*1164insG