Canonical Allele Identifier: CA2579582931
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795890_37795915del , CM000685.2:g.37795890_37795915del GRCh38
NC_000023.10:g.37655143_37655168del , CM000685.1:g.37655143_37655168del GRCh37
NC_000023.9:g.37540083_37540108del NCBI36
NG_009065.1:g.20870_20895del , LRG_53:g.20870_20895del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-61_338-36del ENSP00000512461.1:n.338-61_338-36del
ENST00000696171.1:c.388-61_388-36del ENSP00000512462.1:n.388-61_388-36del
ENST00000696172.1:c.338-3065_338-3040del ENSP00000512463.1:n.338-3065_338-3040del
ENST00000378588.5:c.484-61_484-36del MANE Select ENSP00000367851.4:n.484-61_484-36del
ENST00000378588.4:c.484-61_484-36del ENSP00000367851.4:n.484-61_484-36del
ENST00000465127.1:c.171+369890_171+369915del ENSP00000417050.1:n.171+369890_171+369915del
NM_000397.3:c.484-61_484-36del , LRG_53t1:c.484-61_484-36del NP_000388.2:n.484-61_484-36del
XM_011543890.1:c.178-61_178-36del XP_011542192.1:n.178-61_178-36del
NM_000397.4:c.484-61_484-36del MANE Select NP_000388.2:n.484-61_484-36del