Canonical Allele Identifier: CA2551363469
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796254del , CM000685.2:g.37796254del GRCh38
NC_000023.10:g.37655507del , CM000685.1:g.37655507del GRCh37
NC_000023.9:g.37540447del NCBI36
NG_009065.1:g.21234del , LRG_53:g.21234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*183+113del ENSP00000512461.1:n.*183+113del
ENST00000696171.1:c.578+113del ENSP00000512462.1:n.578+113del
ENST00000696172.1:c.338-2701del ENSP00000512463.1:n.338-2701del
ENST00000378588.5:c.674+113del MANE Select ENSP00000367851.4:n.674+113del
ENST00000378588.4:c.674+113del ENSP00000367851.4:n.674+113del
ENST00000465127.1:c.171+370254del ENSP00000417050.1:n.171+370254del
NM_000397.3:c.674+113del , LRG_53t1:c.674+113del NP_000388.2:n.674+113del
XM_011543890.1:c.368+113del XP_011542192.1:n.368+113del
NM_000397.4:c.674+113del MANE Select NP_000388.2:n.674+113del