Canonical Allele Identifier: CA2820471499
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795894del , CM000685.2:g.37795894del GRCh38
NC_000023.10:g.37655147del , CM000685.1:g.37655147del GRCh37
NC_000023.9:g.37540087del NCBI36
NG_009065.1:g.20874del , LRG_53:g.20874del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-57del ENSP00000512461.1:n.338-57del
ENST00000696171.1:c.388-57del ENSP00000512462.1:n.388-57del
ENST00000696172.1:c.338-3061del ENSP00000512463.1:n.338-3061del
ENST00000378588.5:c.484-57del MANE Select ENSP00000367851.4:n.484-57del
ENST00000378588.4:c.484-57del ENSP00000367851.4:n.484-57del
ENST00000465127.1:c.171+369894del ENSP00000417050.1:n.171+369894del
NM_000397.3:c.484-57del , LRG_53t1:c.484-57del NP_000388.2:n.484-57del
XM_011543890.1:c.178-57del XP_011542192.1:n.178-57del
NM_000397.4:c.484-57del MANE Select NP_000388.2:n.484-57del