Canonical Allele Identifier: CA412977618

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664264C>A (hg19) ; chrX:g.37805011C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805011C>A , CM000685.2:g.37805011C>A	GRCh38
NC_000023.10:g.37664264C>A , CM000685.1:g.37664264C>A	GRCh37
NC_000023.9:g.37549208C>A	NCBI36
NG_009065.1:g.29995C>A , LRG_53:g.29995C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*666C>A	ENSP00000512461.1:n.*666C>A
ENST00000696171.1:c.1061C>A	ENSP00000512462.1:p.Ala354Glu
ENST00000378588.5:c.1157C>A MANE Select	ENSP00000367851.4:p.Ala386Glu
ENST00000378588.4:c.1157C>A	ENSP00000367851.4:p.Ala386Glu
ENST00000465127.1:c.171+379011C>A	ENSP00000417050.1:n.171+379011C>A
NM_000397.3:c.1157C>A , LRG_53t1:c.1157C>A	NP_000388.2:p.Ala386Glu
XM_011543890.1:c.851C>A	XP_011542192.1:p.Ala284Glu
NM_000397.4:c.1157C>A MANE Select	NP_000388.2:p.Ala386Glu