Canonical Allele Identifier: CA2693426507

Gene: CYBB

Linked Data

• gnomAD v4: X-37803728-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803728A>T , CM000685.2:g.37803728A>T	GRCh38
NC_000023.10:g.37662981A>T , CM000685.1:g.37662981A>T	GRCh37
NC_000023.9:g.37547925A>T	NCBI36
NG_009065.1:g.28712A>T , LRG_53:g.28712A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*407-149A>T	ENSP00000512461.1:n.*407-149A>T
ENST00000696171.1:c.802-149A>T	ENSP00000512462.1:n.802-149A>T
ENST00000378588.5:c.898-149A>T MANE Select	ENSP00000367851.4:n.898-149A>T
ENST00000378588.4:c.898-149A>T	ENSP00000367851.4:n.898-149A>T
ENST00000465127.1:c.171+377728A>T	ENSP00000417050.1:n.171+377728A>T
ENST00000492288.1:n.323-149A>T
NM_000397.3:c.898-149A>T , LRG_53t1:c.898-149A>T	NP_000388.2:n.898-149A>T
XM_011543890.1:c.592-149A>T	XP_011542192.1:n.592-149A>T
NM_000397.4:c.898-149A>T MANE Select	NP_000388.2:n.898-149A>T