Canonical Allele Identifier: CA2820471512

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795938_37795939insGTGTA , CM000685.2:g.37795938_37795939insGTGTA	GRCh38
NC_000023.10:g.37655191_37655192insGTGTA , CM000685.1:g.37655191_37655192insGTGTA	GRCh37
NC_000023.9:g.37540131_37540132insGTGTA	NCBI36
NG_009065.1:g.20918_20919insGTGTA , LRG_53:g.20918_20919insGTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-13_338-12insGTGTA	ENSP00000512461.1:n.338-13_338-12insGTGTA
ENST00000696171.1:c.388-13_388-12insGTGTA	ENSP00000512462.1:n.388-13_388-12insGTGTA
ENST00000696172.1:c.338-3017_338-3016insGTGTA	ENSP00000512463.1:n.338-3017_338-3016insGTGTA
ENST00000378588.5:c.484-13_484-12insGTGTA MANE Select	ENSP00000367851.4:n.484-13_484-12insGTGTA
ENST00000378588.4:c.484-13_484-12insGTGTA	ENSP00000367851.4:n.484-13_484-12insGTGTA
ENST00000465127.1:c.171+369938_171+369939insGTGTA	ENSP00000417050.1:n.171+369938_171+369939insGTGTA
NM_000397.3:c.484-13_484-12insGTGTA , LRG_53t1:c.484-13_484-12insGTGTA	NP_000388.2:n.484-13_484-12insGTGTA
XM_011543890.1:c.178-13_178-12insGTGTA	XP_011542192.1:n.178-13_178-12insGTGTA
NM_000397.4:c.484-13_484-12insGTGTA MANE Select	NP_000388.2:n.484-13_484-12insGTGTA