Canonical Allele Identifier: CA2585218317
Gene: CYP2B6 HGNC NCBI

Linked Data

gnomAD v4: 19-41018281-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018283del , CM000681.2:g.41018283del GRCh38
NC_000019.9:g.41524188del , CM000681.1:g.41524188del GRCh37
NC_000019.8:g.46216028del NCBI36
NG_007929.1:g.31985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1456del MANE Select ENSP00000324648.2:n.*1456del
ENST00000324071.8:c.*1456del ENSP00000324648.2:n.*1456del
NM_000767.4:c.*1456del NP_000758.1:n.*1456del
XM_011526548.1:c.*1456del XP_011524850.1:n.*1456del
XM_011526549.1:c.*1456del XP_011524851.1:n.*1456del
XM_011526550.1:c.*1456del XP_011524852.1:n.*1456del
NM_000767.5:c.*1456del MANE Select NP_000758.1:n.*1456del
Search 100 bp 5'
Search 100 bp 3'