Canonical Allele Identifier: CA2336263419
Gene: CYP2B6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018305G= , CM000681.2:g.41018305G= GRCh38
NC_000019.9:g.41524210G= , CM000681.1:g.41524210G= GRCh37
NC_000019.8:g.46216050G= NCBI36
NG_007929.1:g.32007G=

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.*1478G= MANE Select ENSP00000324648.2:n.*1478G=
ENST00000324071.8:c.*1478G= ENSP00000324648.2:n.*1478G=
NM_000767.4:c.*1478G= NP_000758.1:n.*1478G=
XM_011526548.1:c.*1478G= XP_011524850.1:n.*1478G=
XM_011526549.1:c.*1478G= XP_011524851.1:n.*1478G=
XM_011526550.1:c.*1478G= XP_011524852.1:n.*1478G=
NM_000767.5:c.*1478G= MANE Select NP_000758.1:n.*1478G=
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