Canonical Allele Identifier: CA2820471503

Gene: CYBB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795907_37795908insCTGT , CM000685.2:g.37795907_37795908insCTGT	GRCh38
NC_000023.10:g.37655160_37655161insCTGT , CM000685.1:g.37655160_37655161insCTGT	GRCh37
NC_000023.9:g.37540100_37540101insCTGT	NCBI36
NG_009065.1:g.20887_20888insCTGT , LRG_53:g.20887_20888insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-44_338-43insCTGT	ENSP00000512461.1:n.338-44_338-43insCTGT
ENST00000696171.1:c.388-44_388-43insCTGT	ENSP00000512462.1:n.388-44_388-43insCTGT
ENST00000696172.1:c.338-3048_338-3047insCTGT	ENSP00000512463.1:n.338-3048_338-3047insCTGT
ENST00000378588.5:c.484-44_484-43insCTGT MANE Select	ENSP00000367851.4:n.484-44_484-43insCTGT
ENST00000378588.4:c.484-44_484-43insCTGT	ENSP00000367851.4:n.484-44_484-43insCTGT
ENST00000465127.1:c.171+369907_171+369908insCTGT	ENSP00000417050.1:n.171+369907_171+369908insCTGT
NM_000397.3:c.484-44_484-43insCTGT , LRG_53t1:c.484-44_484-43insCTGT	NP_000388.2:n.484-44_484-43insCTGT
XM_011543890.1:c.178-44_178-43insCTGT	XP_011542192.1:n.178-44_178-43insCTGT
NM_000397.4:c.484-44_484-43insCTGT MANE Select	NP_000388.2:n.484-44_484-43insCTGT