Canonical Allele Identifier: CA9455439
Gene: CYP2B6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225985
dbSNP Id: rs28399499

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012316T>C , CM000681.2:g.41012316T>C GRCh38
NC_000019.9:g.41518221T>C , CM000681.1:g.41518221T>C GRCh37
NC_000019.8:g.46210061T>C NCBI36
NG_007929.1:g.26018T>C

Transcript Alleles

HGVS Amino-acid change
NM_000767.4:c.983T>C VV NP_000758.1:p.Ile328Thr
XM_005258569.3:c.983T>C XP_005258626.1:p.Ile328Thr
XM_006723050.2:c.983T>C XP_006723113.1:p.Ile328Thr
XM_011526546.1:c.983T>C XP_011524848.1:p.Ile328Thr
XM_011526547.1:c.983T>C XP_011524849.1:p.Ile328Thr
XM_011526548.1:c.503T>C XP_011524850.1:p.Ile168Thr
XM_011526549.1:c.392T>C XP_011524851.1:p.Ile131Thr
XM_011526550.1:c.383T>C XP_011524852.1:p.Ile128Thr
NM_000767.5:c.983T>C VV NP_000758.1:p.Ile328Thr
ENST00000324071.8:c.983T>C ENSP00000324648.2:p.Ile328Thr
ENST00000593831.1:c.275T>C ENSP00000470582.1:p.Ile92Thr
ENST00000597612.1:n.478T>C