Canonical Allele Identifier: CA2336263414
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018279_41018280delinsCT , CM000681.2:g.41018279_41018280delinsCT GRCh38
NC_000019.9:g.41524184_41524185delinsCT , CM000681.1:g.41524184_41524185delinsCT GRCh37
NC_000019.8:g.46216024_46216025delinsCT NCBI36
NG_007929.1:g.31981_31982delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.*1452_*1453delinsCT MANE Select ENSP00000324648.2:n.*1452_*1453delinsCT
ENST00000324071.8:c.*1452_*1453delinsCT ENSP00000324648.2:n.*1452_*1453delinsCT
NM_000767.4:c.*1452_*1453delinsCT NP_000758.1:n.*1452_*1453delinsCT
XM_011526548.1:c.*1452_*1453delinsCT XP_011524850.1:n.*1452_*1453delinsCT
XM_011526549.1:c.*1452_*1453delinsCT XP_011524851.1:n.*1452_*1453delinsCT
XM_011526550.1:c.*1452_*1453delinsCT XP_011524852.1:n.*1452_*1453delinsCT
NM_000767.5:c.*1452_*1453delinsCT MANE Select NP_000758.1:n.*1452_*1453delinsCT