Canonical Allele Identifier: CA412977013

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37663133G>A (hg19) ; chrX:g.37803880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803880G>A , CM000685.2:g.37803880G>A	GRCh38
NC_000023.10:g.37663133G>A , CM000685.1:g.37663133G>A	GRCh37
NC_000023.9:g.37548077G>A	NCBI36
NG_009065.1:g.28864G>A , LRG_53:g.28864G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*410G>A	ENSP00000512461.1:n.*410G>A
ENST00000696171.1:c.805G>A	ENSP00000512462.1:p.Val269Ile
ENST00000378588.5:c.901G>A MANE Select	ENSP00000367851.4:p.Val301Ile
ENST00000378588.4:c.901G>A	ENSP00000367851.4:p.Val301Ile
ENST00000465127.1:c.171+377880G>A	ENSP00000417050.1:n.171+377880G>A
ENST00000492288.1:n.326G>A
NM_000397.3:c.901G>A , LRG_53t1:c.901G>A	NP_000388.2:p.Val301Ile
XM_011543890.1:c.595G>A	XP_011542192.1:p.Val199Ile
NM_000397.4:c.901G>A MANE Select	NP_000388.2:p.Val301Ile