Canonical Allele Identifier: CA405984836
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1235476472

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012475T>C , CM000681.2:g.41012475T>C GRCh38
NC_000019.9:g.41518380T>C , CM000681.1:g.41518380T>C GRCh37
NC_000019.8:g.46210220T>C NCBI36
NG_007929.1:g.26177T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1142T>C MANE Select ENSP00000324648.2:p.Ile381Thr
ENST00000598834.2:c.1166T>C
ENST00000324071.8:c.1142T>C ENSP00000324648.2:p.Ile381Thr
ENST00000593831.1:c.434T>C ENSP00000470582.1:p.Ile145Thr
ENST00000597612.1:n.637T>C
NM_000767.4:c.1142T>C NP_000758.1:p.Ile381Thr
XM_005258569.3:c.1142T>C XP_005258626.1:p.Ile381Thr
XM_006723050.2:c.1142T>C XP_006723113.1:p.Ile381Thr
XM_011526546.1:c.1142T>C XP_011524848.1:p.Ile381Thr
XM_011526547.1:c.1142T>C XP_011524849.1:p.Ile381Thr
XM_011526548.1:c.662T>C XP_011524850.1:p.Ile221Thr
XM_011526549.1:c.551T>C XP_011524851.1:p.Ile184Thr
XM_011526550.1:c.542T>C XP_011524852.1:p.Ile181Thr
NM_000767.5:c.1142T>C MANE Select NP_000758.1:p.Ile381Thr