Canonical Allele Identifier: CA2695232432
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783508_37783513del , CM000685.2:g.37783508_37783513del GRCh38
NC_000023.10:g.37642761_37642766del , CM000685.1:g.37642761_37642766del GRCh37
NC_000023.9:g.37527705_37527710del NCBI36
NG_009065.1:g.8492_8497del , LRG_53:g.8492_8497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.160_165del ENSP00000512461.1:p.Arg54_Ala55del
ENST00000696171.1:c.64_69del ENSP00000512462.1:p.Arg22_Ala23del
ENST00000696172.1:c.160_165del ENSP00000512463.1:p.Arg54_Ala55del
ENST00000696173.1:n.168_173del
ENST00000378588.5:c.160_165del MANE Select ENSP00000367851.4:p.Arg54_Ala55del
ENST00000378588.4:c.160_165del ENSP00000367851.4:p.Arg54_Ala55del
ENST00000465127.1:c.171+357508_171+357513del ENSP00000417050.1:n.171+357508_171+357513del
NM_000397.3:c.160_165del , LRG_53t1:c.160_165del NP_000388.2:p.Arg54_Ala55del
XM_011543890.1:c.-271_-266del XP_011542192.1:n.-271_-266del
NM_000397.4:c.160_165del MANE Select NP_000388.2:p.Arg54_Ala55del