Canonical Allele Identifier: CA2585218160
Gene: CYP2B6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41017956A>G , CM000681.2:g.41017956A>G GRCh38
NC_000019.9:g.41523861A>G , CM000681.1:g.41523861A>G GRCh37
NC_000019.8:g.46215701A>G NCBI36
NG_007929.1:g.31658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1129A>G MANE Select ENSP00000324648.2:n.*1129A>G
ENST00000324071.8:c.*1129A>G ENSP00000324648.2:n.*1129A>G
NM_000767.4:c.*1129A>G NP_000758.1:n.*1129A>G
XM_011526548.1:c.*1129A>G XP_011524850.1:n.*1129A>G
XM_011526549.1:c.*1129A>G XP_011524851.1:n.*1129A>G
XM_011526550.1:c.*1129A>G XP_011524852.1:n.*1129A>G
NM_000767.5:c.*1129A>G MANE Select NP_000758.1:n.*1129A>G