Canonical Allele Identifier: CA1132390566

Gene: CYBB

Linked Data

• dbSNP Id: rs1929293601
• gnomAD v3: X-37795915-T-TGTGTGG
• gnomAD v4: X-37795915-T-TGTGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795920_37795921insGGTGTG , CM000685.2:g.37795920_37795921insGGTGTG	GRCh38
NC_000023.10:g.37655173_37655174insGGTGTG , CM000685.1:g.37655173_37655174insGGTGTG	GRCh37
NC_000023.9:g.37540113_37540114insGGTGTG	NCBI36
NG_009065.1:g.20900_20901insGGTGTG , LRG_53:g.20900_20901insGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-31_338-30insGGTGTG	ENSP00000512461.1:n.338-31_338-30insGGTGTG
ENST00000696171.1:c.388-31_388-30insGGTGTG	ENSP00000512462.1:n.388-31_388-30insGGTGTG
ENST00000696172.1:c.338-3035_338-3034insGGTGTG	ENSP00000512463.1:n.338-3035_338-3034insGGTGTG
ENST00000378588.5:c.484-31_484-30insGGTGTG MANE Select	ENSP00000367851.4:n.484-31_484-30insGGTGTG
ENST00000378588.4:c.484-31_484-30insGGTGTG	ENSP00000367851.4:n.484-31_484-30insGGTGTG
ENST00000465127.1:c.171+369920_171+369921insGGTGTG	ENSP00000417050.1:n.171+369920_171+369921insGGTGTG
NM_000397.3:c.484-31_484-30insGGTGTG , LRG_53t1:c.484-31_484-30insGGTGTG	NP_000388.2:n.484-31_484-30insGGTGTG
XM_011543890.1:c.178-31_178-30insGGTGTG	XP_011542192.1:n.178-31_178-30insGGTGTG
NM_000397.4:c.484-31_484-30insGGTGTG MANE Select	NP_000388.2:n.484-31_484-30insGGTGTG