Canonical Allele Identifier: CA2693426555

Gene: CYBB

Linked Data

• gnomAD v4: X-37803826-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803826G>A , CM000685.2:g.37803826G>A	GRCh38
NC_000023.10:g.37663079G>A , CM000685.1:g.37663079G>A	GRCh37
NC_000023.9:g.37548023G>A	NCBI36
NG_009065.1:g.28810G>A , LRG_53:g.28810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*407-51G>A	ENSP00000512461.1:n.*407-51G>A
ENST00000696171.1:c.802-51G>A	ENSP00000512462.1:n.802-51G>A
ENST00000378588.5:c.898-51G>A MANE Select	ENSP00000367851.4:n.898-51G>A
ENST00000378588.4:c.898-51G>A	ENSP00000367851.4:n.898-51G>A
ENST00000465127.1:c.171+377826G>A	ENSP00000417050.1:n.171+377826G>A
ENST00000492288.1:n.323-51G>A
NM_000397.3:c.898-51G>A , LRG_53t1:c.898-51G>A	NP_000388.2:n.898-51G>A
XM_011543890.1:c.592-51G>A	XP_011542192.1:n.592-51G>A
NM_000397.4:c.898-51G>A MANE Select	NP_000388.2:n.898-51G>A