Canonical Allele Identifier: CA219722

Gene: CYBB

Linked Data

• ClinVar Variation Id: 68395
• ClinVar RCV Id: RCV000059261
• dbSNP Id: rs151344491
• MyVariant Identifiers: chrX:g.37655255G>A (hg19) ; chrX:g.37796002G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796002G>A , CM000685.2:g.37796002G>A	GRCh38
NC_000023.10:g.37655255G>A , CM000685.1:g.37655255G>A	GRCh37
NC_000023.9:g.37540195G>A	NCBI36
NG_009065.1:g.20982G>A , LRG_53:g.20982G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*44G>A	ENSP00000512461.1:n.*44G>A
ENST00000696171.1:c.439G>A	ENSP00000512462.1:p.Gly147Arg
ENST00000696172.1:c.338-2953G>A	ENSP00000512463.1:n.338-2953G>A
ENST00000378588.5:c.535G>A MANE Select	ENSP00000367851.4:p.Gly179Arg
ENST00000378588.4:c.535G>A	ENSP00000367851.4:p.Gly179Arg
ENST00000465127.1:c.171+370002G>A	ENSP00000417050.1:n.171+370002G>A
NM_000397.3:c.535G>A , LRG_53t1:c.535G>A	NP_000388.2:p.Gly179Arg
XM_011543890.1:c.229G>A	XP_011542192.1:p.Gly77Arg
NM_000397.4:c.535G>A MANE Select	NP_000388.2:p.Gly179Arg