Canonical Allele Identifier: CA2424676657

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783911_37783912delinsCT , CM000685.2:g.37783911_37783912delinsCT	GRCh38
NC_000023.10:g.37643164_37643165delinsCT , CM000685.1:g.37643164_37643165delinsCT	GRCh37
NC_000023.9:g.37528108_37528109delinsCT	NCBI36
NG_009065.1:g.8895_8896delinsCT , LRG_53:g.8895_8896delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+311_252+312delinsCT	ENSP00000512461.1:n.252+311_252+312delinsCT
ENST00000696171.1:c.156+311_156+312delinsCT	ENSP00000512462.1:n.156+311_156+312delinsCT
ENST00000696172.1:c.252+311_252+312delinsCT	ENSP00000512463.1:n.252+311_252+312delinsCT
ENST00000696173.1:n.260+311_260+312delinsCT
ENST00000378588.5:c.252+311_252+312delinsCT MANE Select	ENSP00000367851.4:n.252+311_252+312delinsCT
ENST00000378588.4:c.252+311_252+312delinsCT	ENSP00000367851.4:n.252+311_252+312delinsCT
ENST00000465127.1:c.171+357911_171+357912delinsCT	ENSP00000417050.1:n.171+357911_171+357912delinsCT
NM_000397.3:c.252+311_252+312delinsCT , LRG_53t1:c.252+311_252+312delinsCT	NP_000388.2:n.252+311_252+312delinsCT
XM_011543890.1:c.-179+311_-179+312delinsCT	XP_011542192.1:n.-179+311_-179+312delinsCT
NM_000397.4:c.252+311_252+312delinsCT MANE Select	NP_000388.2:n.252+311_252+312delinsCT