Canonical Allele Identifier: CA2820471495
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795893_37795895del , CM000685.2:g.37795893_37795895del GRCh38
NC_000023.10:g.37655146_37655148del , CM000685.1:g.37655146_37655148del GRCh37
NC_000023.9:g.37540086_37540088del NCBI36
NG_009065.1:g.20873_20875del , LRG_53:g.20873_20875del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-58_338-56del ENSP00000512461.1:n.338-58_338-56del
ENST00000696171.1:c.388-58_388-56del ENSP00000512462.1:n.388-58_388-56del
ENST00000696172.1:c.338-3062_338-3060del ENSP00000512463.1:n.338-3062_338-3060del
ENST00000378588.5:c.484-58_484-56del MANE Select ENSP00000367851.4:n.484-58_484-56del
ENST00000378588.4:c.484-58_484-56del ENSP00000367851.4:n.484-58_484-56del
ENST00000465127.1:c.171+369893_171+369895del ENSP00000417050.1:n.171+369893_171+369895del
NM_000397.3:c.484-58_484-56del , LRG_53t1:c.484-58_484-56del NP_000388.2:n.484-58_484-56del
XM_011543890.1:c.178-58_178-56del XP_011542192.1:n.178-58_178-56del
NM_000397.4:c.484-58_484-56del MANE Select NP_000388.2:n.484-58_484-56del