Canonical Allele Identifier: CA412977786

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664342G>A (hg19) ; chrX:g.37805089G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805089G>A , CM000685.2:g.37805089G>A	GRCh38
NC_000023.10:g.37664342G>A , CM000685.1:g.37664342G>A	GRCh37
NC_000023.9:g.37549286G>A	NCBI36
NG_009065.1:g.30073G>A , LRG_53:g.30073G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*744G>A	ENSP00000512461.1:n.*744G>A
ENST00000696171.1:c.1139G>A	ENSP00000512462.1:p.Gly380Glu
ENST00000378588.5:c.1235G>A MANE Select	ENSP00000367851.4:p.Gly412Glu
ENST00000378588.4:c.1235G>A	ENSP00000367851.4:p.Gly412Glu
ENST00000465127.1:c.171+379089G>A	ENSP00000417050.1:n.171+379089G>A
NM_000397.3:c.1235G>A , LRG_53t1:c.1235G>A	NP_000388.2:p.Gly412Glu
XM_011543890.1:c.929G>A	XP_011542192.1:p.Gly310Glu
NM_000397.4:c.1235G>A MANE Select	NP_000388.2:p.Gly412Glu