Canonical Allele Identifier: CA16621365
Gene: CYBB HGNC NCBI

Linked Data

ClinVar Variation Id: 419755
ClinVar RCV Id: RCV000479844
dbSNP Id: rs1064794086

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37782127del , CM000685.2:g.37782127del GRCh38
NC_000023.10:g.37641380del , CM000685.1:g.37641380del GRCh37
NC_000023.9:g.37526324del NCBI36
NG_009065.1:g.7111del , LRG_53:g.7111del

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.85del ENSP00000512461.1:p.Tyr29IlefsTer?
ENST00000696171.1:c.46-1363del ENSP00000512462.1:n.46-1363del
ENST00000696172.1:c.85del ENSP00000512463.1:p.Tyr29IlefsTer?
ENST00000696173.1:n.93del
ENST00000378588.5:c.85del MANE Select ENSP00000367851.4:p.Tyr29IlefsTer?
ENST00000378588.4:c.85del ENSP00000367851.4:p.Tyr29IlefsTer?
ENST00000465127.1:c.171+356127del ENSP00000417050.1:n.171+356127del
NM_000397.3:c.85del , LRG_53t1:c.85del NP_000388.2:p.Tyr29IlefsTer?
XM_011543890.1:c.-346del XP_011542192.1:n.-346del
NM_000397.4:c.85del MANE Select NP_000388.2:p.Tyr29IlefsTer?