Canonical Allele Identifier: CA2336263349
Gene: CYP2B6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018103C= , CM000681.2:g.41018103C= GRCh38
NC_000019.9:g.41524008C= , CM000681.1:g.41524008C= GRCh37
NC_000019.8:g.46215848C= NCBI36
NG_007929.1:g.31805C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1276C= MANE Select ENSP00000324648.2:n.*1276C=
ENST00000324071.8:c.*1276C= ENSP00000324648.2:n.*1276C=
NM_000767.4:c.*1276C= NP_000758.1:n.*1276C=
XM_011526548.1:c.*1276C= XP_011524850.1:n.*1276C=
XM_011526549.1:c.*1276C= XP_011524851.1:n.*1276C=
XM_011526550.1:c.*1276C= XP_011524852.1:n.*1276C=
NM_000767.5:c.*1276C= MANE Select NP_000758.1:n.*1276C=
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