Canonical Allele Identifier: CA2424676663
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783925_37783927delinsCAT , CM000685.2:g.37783925_37783927delinsCAT GRCh38
NC_000023.10:g.37643178_37643180delinsCAT , CM000685.1:g.37643178_37643180delinsCAT GRCh37
NC_000023.9:g.37528122_37528124delinsCAT NCBI36
NG_009065.1:g.8909_8911delinsCAT , LRG_53:g.8909_8911delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+325_252+327delinsCAT ENSP00000512461.1:n.252+325_252+327delinsCAT
ENST00000696171.1:c.156+325_156+327delinsCAT ENSP00000512462.1:n.156+325_156+327delinsCAT
ENST00000696172.1:c.252+325_252+327delinsCAT ENSP00000512463.1:n.252+325_252+327delinsCAT
ENST00000696173.1:n.260+325_260+327delinsCAT
ENST00000378588.5:c.252+325_252+327delinsCAT MANE Select ENSP00000367851.4:n.252+325_252+327delinsCAT
ENST00000378588.4:c.252+325_252+327delinsCAT ENSP00000367851.4:n.252+325_252+327delinsCAT
ENST00000465127.1:c.171+357925_171+357927delinsCAT ENSP00000417050.1:n.171+357925_171+357927delinsCAT
NM_000397.3:c.252+325_252+327delinsCAT , LRG_53t1:c.252+325_252+327delinsCAT NP_000388.2:n.252+325_252+327delinsCAT
XM_011543890.1:c.-179+325_-179+327delinsCAT XP_011542192.1:n.-179+325_-179+327delinsCAT
NM_000397.4:c.252+325_252+327delinsCAT MANE Select NP_000388.2:n.252+325_252+327delinsCAT