Canonical Allele Identifier: CA920110794
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1599855768

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018041del , CM000681.2:g.41018041del GRCh38
NC_000019.9:g.41523946del , CM000681.1:g.41523946del GRCh37
NC_000019.8:g.46215786del NCBI36
NG_007929.1:g.31743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1214del MANE Select ENSP00000324648.2:n.*1214del
ENST00000324071.8:c.*1214del ENSP00000324648.2:n.*1214del
NM_000767.4:c.*1214del NP_000758.1:n.*1214del
XM_011526548.1:c.*1214del XP_011524850.1:n.*1214del
XM_011526549.1:c.*1214del XP_011524851.1:n.*1214del
XM_011526550.1:c.*1214del XP_011524852.1:n.*1214del
NM_000767.5:c.*1214del MANE Select NP_000758.1:n.*1214del