Canonical Allele Identifier: CA2561093127
Gene: CYP2B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018070_41018077del , CM000681.2:g.41018070_41018077del GRCh38
NC_000019.9:g.41523975_41523982del , CM000681.1:g.41523975_41523982del GRCh37
NC_000019.8:g.46215815_46215822del NCBI36
NG_007929.1:g.31772_31779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1243_*1250del MANE Select ENSP00000324648.2:n.*1243_*1250del
ENST00000324071.8:c.*1243_*1250del ENSP00000324648.2:n.*1243_*1250del
NM_000767.4:c.*1243_*1250del NP_000758.1:n.*1243_*1250del
XM_011526548.1:c.*1243_*1250del XP_011524850.1:n.*1243_*1250del
XM_011526549.1:c.*1243_*1250del XP_011524851.1:n.*1243_*1250del
XM_011526550.1:c.*1243_*1250del XP_011524852.1:n.*1243_*1250del
NM_000767.5:c.*1243_*1250del MANE Select NP_000758.1:n.*1243_*1250del