Canonical Allele Identifier: CA2693426587

Gene: CYBB

Linked Data

• gnomAD v4: X-37796204-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796206del , CM000685.2:g.37796206del	GRCh38
NC_000023.10:g.37655459del , CM000685.1:g.37655459del	GRCh37
NC_000023.9:g.37540399del	NCBI36
NG_009065.1:g.21186del , LRG_53:g.21186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*183+65del	ENSP00000512461.1:n.*183+65del
ENST00000696171.1:c.578+65del	ENSP00000512462.1:n.578+65del
ENST00000696172.1:c.338-2749del	ENSP00000512463.1:n.338-2749del
ENST00000378588.5:c.674+65del MANE Select	ENSP00000367851.4:n.674+65del
ENST00000378588.4:c.674+65del	ENSP00000367851.4:n.674+65del
ENST00000465127.1:c.171+370206del	ENSP00000417050.1:n.171+370206del
NM_000397.3:c.674+65del , LRG_53t1:c.674+65del	NP_000388.2:n.674+65del
XM_011543890.1:c.368+65del	XP_011542192.1:n.368+65del
NM_000397.4:c.674+65del MANE Select	NP_000388.2:n.674+65del