Canonical Allele Identifier: CA14643177
Gene: CYP2B6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1042389

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018248T>C , CM000681.2:g.41018248T>C GRCh38
NC_000019.9:g.41524153T>C , CM000681.1:g.41524153T>C GRCh37
NC_000019.8:g.46215993T>C NCBI36
NG_007929.1:g.31950T>C

Transcript Alleles

HGVS Amino-acid change
NM_000767.4:c.*1421T>C VV NP_000758.1:p.=
XM_011526548.1:c.*1421T>C XP_011524850.1:p.=
XM_011526549.1:c.*1421T>C XP_011524851.1:p.=
XM_011526550.1:c.*1421T>C XP_011524852.1:p.=
NM_000767.5:c.*1421T>C VV
ENST00000324071.8:c.*1421T>C ENSP00000324648.2:p.=