Canonical Allele Identifier: CA412977128

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37663183C>A (hg19) ; chrX:g.37803930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803930C>A , CM000685.2:g.37803930C>A	GRCh38
NC_000023.10:g.37663183C>A , CM000685.1:g.37663183C>A	GRCh37
NC_000023.9:g.37548127C>A	NCBI36
NG_009065.1:g.28914C>A , LRG_53:g.28914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*460C>A	ENSP00000512461.1:n.*460C>A
ENST00000696171.1:c.855C>A	ENSP00000512462.1:p.Phe285Leu
ENST00000378588.5:c.951C>A MANE Select	ENSP00000367851.4:p.Phe317Leu
ENST00000378588.4:c.951C>A	ENSP00000367851.4:p.Phe317Leu
ENST00000465127.1:c.171+377930C>A	ENSP00000417050.1:n.171+377930C>A
ENST00000492288.1:n.376C>A
NM_000397.3:c.951C>A , LRG_53t1:c.951C>A	NP_000388.2:p.Phe317Leu
XM_011543890.1:c.645C>A	XP_011542192.1:p.Phe215Leu
NM_000397.4:c.951C>A MANE Select	NP_000388.2:p.Phe317Leu