Canonical Allele Identifier: CA2693426361

Gene: CYBB

Linked Data

• gnomAD v4: X-37795890-A-ATGTGTGTGTGTGTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795922_37795937dup , CM000685.2:g.37795922_37795937dup	GRCh38
NC_000023.10:g.37655175_37655190dup , CM000685.1:g.37655175_37655190dup	GRCh37
NC_000023.9:g.37540115_37540130dup	NCBI36
NG_009065.1:g.20902_20917dup , LRG_53:g.20902_20917dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-29_338-14dup	ENSP00000512461.1:n.338-29_338-14dup
ENST00000696171.1:c.388-29_388-14dup	ENSP00000512462.1:n.388-29_388-14dup
ENST00000696172.1:c.338-3033_338-3018dup	ENSP00000512463.1:n.338-3033_338-3018dup
ENST00000378588.5:c.484-29_484-14dup MANE Select	ENSP00000367851.4:n.484-29_484-14dup
ENST00000378588.4:c.484-29_484-14dup	ENSP00000367851.4:n.484-29_484-14dup
ENST00000465127.1:c.171+369922_171+369937dup	ENSP00000417050.1:n.171+369922_171+369937dup
NM_000397.3:c.484-29_484-14dup , LRG_53t1:c.484-29_484-14dup	NP_000388.2:n.484-29_484-14dup
XM_011543890.1:c.178-29_178-14dup	XP_011542192.1:n.178-29_178-14dup
NM_000397.4:c.484-29_484-14dup MANE Select	NP_000388.2:n.484-29_484-14dup