Canonical Allele Identifier: CA2424680325

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795889_37795895delinsCATGTGT , CM000685.2:g.37795889_37795895delinsCATGTGT	GRCh38
NC_000023.10:g.37655142_37655148delinsCATGTGT , CM000685.1:g.37655142_37655148delinsCATGTGT	GRCh37
NC_000023.9:g.37540082_37540088delinsCATGTGT	NCBI36
NG_009065.1:g.20869_20875delinsCATGTGT , LRG_53:g.20869_20875delinsCATGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-62_338-56delinsCATGTGT	ENSP00000512461.1:n.338-62_338-56delinsCATGTGT
ENST00000696171.1:c.388-62_388-56delinsCATGTGT	ENSP00000512462.1:n.388-62_388-56delinsCATGTGT
ENST00000696172.1:c.338-3066_338-3060delinsCATGTGT	ENSP00000512463.1:n.338-3066_338-3060delinsCATGTGT
ENST00000378588.5:c.484-62_484-56delinsCATGTGT MANE Select	ENSP00000367851.4:n.484-62_484-56delinsCATGTGT
ENST00000378588.4:c.484-62_484-56delinsCATGTGT	ENSP00000367851.4:n.484-62_484-56delinsCATGTGT
ENST00000465127.1:c.171+369889_171+369895delinsCATGTGT	ENSP00000417050.1:n.171+369889_171+369895delinsCATGTGT
NM_000397.3:c.484-62_484-56delinsCATGTGT , LRG_53t1:c.484-62_484-56delinsCATGTGT	NP_000388.2:n.484-62_484-56delinsCATGTGT
XM_011543890.1:c.178-62_178-56delinsCATGTGT	XP_011542192.1:n.178-62_178-56delinsCATGTGT
NM_000397.4:c.484-62_484-56delinsCATGTGT MANE Select	NP_000388.2:n.484-62_484-56delinsCATGTGT