Canonical Allele Identifier: CA2336263389
Gene: CYP2B6 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018216A= , CM000681.2:g.41018216A= GRCh38
NC_000019.9:g.41524121A= , CM000681.1:g.41524121A= GRCh37
NC_000019.8:g.46215961A= NCBI36
NG_007929.1:g.31918A=

Transcript Alleles

HGVS Amino-acid change
ENST00000324071.10:c.*1389A= MANE Select ENSP00000324648.2:n.*1389A=
ENST00000324071.8:c.*1389A= ENSP00000324648.2:n.*1389A=
NM_000767.4:c.*1389A= NP_000758.1:n.*1389A=
XM_011526548.1:c.*1389A= XP_011524850.1:n.*1389A=
XM_011526549.1:c.*1389A= XP_011524851.1:n.*1389A=
XM_011526550.1:c.*1389A= XP_011524852.1:n.*1389A=
NM_000767.5:c.*1389A= MANE Select NP_000758.1:n.*1389A=
Search 100 bp 5'
Search 100 bp 3'