Canonical Allele Identifier: CA2424676636
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783877_37783879delinsCAT , CM000685.2:g.37783877_37783879delinsCAT GRCh38
NC_000023.10:g.37643130_37643132delinsCAT , CM000685.1:g.37643130_37643132delinsCAT GRCh37
NC_000023.9:g.37528074_37528076delinsCAT NCBI36
NG_009065.1:g.8861_8863delinsCAT , LRG_53:g.8861_8863delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+277_252+279delinsCAT ENSP00000512461.1:n.252+277_252+279delinsCAT
ENST00000696171.1:c.156+277_156+279delinsCAT ENSP00000512462.1:n.156+277_156+279delinsCAT
ENST00000696172.1:c.252+277_252+279delinsCAT ENSP00000512463.1:n.252+277_252+279delinsCAT
ENST00000696173.1:n.260+277_260+279delinsCAT
ENST00000378588.5:c.252+277_252+279delinsCAT MANE Select ENSP00000367851.4:n.252+277_252+279delinsCAT
ENST00000378588.4:c.252+277_252+279delinsCAT ENSP00000367851.4:n.252+277_252+279delinsCAT
ENST00000465127.1:c.171+357877_171+357879delinsCAT ENSP00000417050.1:n.171+357877_171+357879delinsCAT
NM_000397.3:c.252+277_252+279delinsCAT , LRG_53t1:c.252+277_252+279delinsCAT NP_000388.2:n.252+277_252+279delinsCAT
XM_011543890.1:c.-179+277_-179+279delinsCAT XP_011542192.1:n.-179+277_-179+279delinsCAT
NM_000397.4:c.252+277_252+279delinsCAT MANE Select NP_000388.2:n.252+277_252+279delinsCAT