Canonical Allele Identifier: CA1139652793
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018279dup , CM000681.2:g.41018279dup GRCh38
NC_000019.9:g.41524184dup , CM000681.1:g.41524184dup GRCh37
NC_000019.8:g.46216024dup NCBI36
NG_007929.1:g.31981dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1452dup MANE Select ENSP00000324648.2:n.*1452dup
ENST00000324071.8:c.*1452dup ENSP00000324648.2:n.*1452dup
NM_000767.4:c.*1452dup NP_000758.1:n.*1452dup
XM_011526548.1:c.*1452dup XP_011524850.1:n.*1452dup
XM_011526549.1:c.*1452dup XP_011524851.1:n.*1452dup
XM_011526550.1:c.*1452dup XP_011524852.1:n.*1452dup
NM_000767.5:c.*1452dup MANE Select NP_000758.1:n.*1452dup