Canonical Allele Identifier: CA2336263394
Gene: CYP2B6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018226A= , CM000681.2:g.41018226A= GRCh38
NC_000019.9:g.41524131A= , CM000681.1:g.41524131A= GRCh37
NC_000019.8:g.46215971A= NCBI36
NG_007929.1:g.31928A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1399A= MANE Select ENSP00000324648.2:n.*1399A=
ENST00000324071.8:c.*1399A= ENSP00000324648.2:n.*1399A=
NM_000767.4:c.*1399A= NP_000758.1:n.*1399A=
XM_011526548.1:c.*1399A= XP_011524850.1:n.*1399A=
XM_011526549.1:c.*1399A= XP_011524851.1:n.*1399A=
XM_011526550.1:c.*1399A= XP_011524852.1:n.*1399A=
NM_000767.5:c.*1399A= MANE Select NP_000758.1:n.*1399A=
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