Canonical Allele Identifier: CA9455613
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs3211371

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41016810C>T , CM000681.2:g.41016810C>T GRCh38
NC_000019.9:g.41522715C>T , CM000681.1:g.41522715C>T GRCh37
NC_000019.8:g.46214555C>T NCBI36
NG_007929.1:g.30512C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.1459C>T MANE Select ENSP00000324648.2:p.Arg487Cys
ENST00000598834.2:c.1399C>T
ENST00000324071.8:c.1459C>T ENSP00000324648.2:p.Arg487Cys
ENST00000593831.1:c.751C>T ENSP00000470582.1:p.Arg251Cys
ENST00000597612.1:n.812C>T
NM_000767.4:c.1459C>T NP_000758.1:p.Arg487Cys
XM_005258569.3:c.*48C>T XP_005258626.1:n.*48C>T
XM_011526548.1:c.979C>T XP_011524850.1:p.Arg327Cys
XM_011526549.1:c.868C>T XP_011524851.1:p.Arg290Cys
XM_011526550.1:c.859C>T XP_011524852.1:p.Arg287Cys
NM_000767.5:c.1459C>T MANE Select NP_000758.1:p.Arg487Cys