Canonical Allele Identifier: CA1132390577

Gene: CYBB

Linked Data

• dbSNP Id: rs1842090623
• gnomAD v3: X-37795920-G-GTC
• gnomAD v4: X-37795920-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795921_37795922insCT , CM000685.2:g.37795921_37795922insCT	GRCh38
NC_000023.10:g.37655174_37655175insCT , CM000685.1:g.37655174_37655175insCT	GRCh37
NC_000023.9:g.37540114_37540115insCT	NCBI36
NG_009065.1:g.20901_20902insCT , LRG_53:g.20901_20902insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-30_338-29insCT	ENSP00000512461.1:n.338-30_338-29insCT
ENST00000696171.1:c.388-30_388-29insCT	ENSP00000512462.1:n.388-30_388-29insCT
ENST00000696172.1:c.338-3034_338-3033insCT	ENSP00000512463.1:n.338-3034_338-3033insCT
ENST00000378588.5:c.484-30_484-29insCT MANE Select	ENSP00000367851.4:n.484-30_484-29insCT
ENST00000378588.4:c.484-30_484-29insCT	ENSP00000367851.4:n.484-30_484-29insCT
ENST00000465127.1:c.171+369921_171+369922insCT	ENSP00000417050.1:n.171+369921_171+369922insCT
NM_000397.3:c.484-30_484-29insCT , LRG_53t1:c.484-30_484-29insCT	NP_000388.2:n.484-30_484-29insCT
XM_011543890.1:c.178-30_178-29insCT	XP_011542192.1:n.178-30_178-29insCT
NM_000397.4:c.484-30_484-29insCT MANE Select	NP_000388.2:n.484-30_484-29insCT