Canonical Allele Identifier: CA2693426420

Gene: CYBB

Linked Data

• gnomAD v4: X-37795933-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795934_37795935insAG , CM000685.2:g.37795934_37795935insAG	GRCh38
NC_000023.10:g.37655187_37655188insAG , CM000685.1:g.37655187_37655188insAG	GRCh37
NC_000023.9:g.37540127_37540128insAG	NCBI36
NG_009065.1:g.20914_20915insAG , LRG_53:g.20914_20915insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-17_338-16insAG	ENSP00000512461.1:n.338-17_338-16insAG
ENST00000696171.1:c.388-17_388-16insAG	ENSP00000512462.1:n.388-17_388-16insAG
ENST00000696172.1:c.338-3021_338-3020insAG	ENSP00000512463.1:n.338-3021_338-3020insAG
ENST00000378588.5:c.484-17_484-16insAG MANE Select	ENSP00000367851.4:n.484-17_484-16insAG
ENST00000378588.4:c.484-17_484-16insAG	ENSP00000367851.4:n.484-17_484-16insAG
ENST00000465127.1:c.171+369934_171+369935insAG	ENSP00000417050.1:n.171+369934_171+369935insAG
NM_000397.3:c.484-17_484-16insAG , LRG_53t1:c.484-17_484-16insAG	NP_000388.2:n.484-17_484-16insAG
XM_011543890.1:c.178-17_178-16insAG	XP_011542192.1:n.178-17_178-16insAG
NM_000397.4:c.484-17_484-16insAG MANE Select	NP_000388.2:n.484-17_484-16insAG