Canonical Allele Identifier: CA2693426535
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803780del , CM000685.2:g.37803780del GRCh38
NC_000023.10:g.37663033del , CM000685.1:g.37663033del GRCh37
NC_000023.9:g.37547977del NCBI36
NG_009065.1:g.28764del , LRG_53:g.28764del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*407-97del ENSP00000512461.1:n.*407-97del
ENST00000696171.1:c.802-97del ENSP00000512462.1:n.802-97del
ENST00000378588.5:c.898-97del MANE Select ENSP00000367851.4:n.898-97del
ENST00000378588.4:c.898-97del ENSP00000367851.4:n.898-97del
ENST00000465127.1:c.171+377780del ENSP00000417050.1:n.171+377780del
ENST00000492288.1:n.323-97del
NM_000397.3:c.898-97del , LRG_53t1:c.898-97del NP_000388.2:n.898-97del
XM_011543890.1:c.592-97del XP_011542192.1:n.592-97del
NM_000397.4:c.898-97del MANE Select NP_000388.2:n.898-97del