Canonical Allele Identifier: CA412977642

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664278T>A (hg19) ; chrX:g.37805025T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805025T>A , CM000685.2:g.37805025T>A	GRCh38
NC_000023.10:g.37664278T>A , CM000685.1:g.37664278T>A	GRCh37
NC_000023.9:g.37549222T>A	NCBI36
NG_009065.1:g.30009T>A , LRG_53:g.30009T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*680T>A	ENSP00000512461.1:n.*680T>A
ENST00000696171.1:c.1075T>A	ENSP00000512462.1:p.Phe359Ile
ENST00000378588.5:c.1171T>A MANE Select	ENSP00000367851.4:p.Phe391Ile
ENST00000378588.4:c.1171T>A	ENSP00000367851.4:p.Phe391Ile
ENST00000465127.1:c.171+379025T>A	ENSP00000417050.1:n.171+379025T>A
NM_000397.3:c.1171T>A , LRG_53t1:c.1171T>A	NP_000388.2:p.Phe391Ile
XM_011543890.1:c.865T>A	XP_011542192.1:p.Phe289Ile
NM_000397.4:c.1171T>A MANE Select	NP_000388.2:p.Phe391Ile