Canonical Allele Identifier: CA412975787

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655216G>A (hg19) ; chrX:g.37795963G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795963G>A , CM000685.2:g.37795963G>A	GRCh38
NC_000023.10:g.37655216G>A , CM000685.1:g.37655216G>A	GRCh37
NC_000023.9:g.37540156G>A	NCBI36
NG_009065.1:g.20943G>A , LRG_53:g.20943G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*5G>A	ENSP00000512461.1:n.*5G>A
ENST00000696171.1:c.400G>A	ENSP00000512462.1:p.Gly134Ser
ENST00000696172.1:c.338-2992G>A	ENSP00000512463.1:n.338-2992G>A
ENST00000378588.5:c.496G>A MANE Select	ENSP00000367851.4:p.Gly166Ser
ENST00000378588.4:c.496G>A	ENSP00000367851.4:p.Gly166Ser
ENST00000465127.1:c.171+369963G>A	ENSP00000417050.1:n.171+369963G>A
NM_000397.3:c.496G>A , LRG_53t1:c.496G>A	NP_000388.2:p.Gly166Ser
XM_011543890.1:c.190G>A	XP_011542192.1:p.Gly64Ser
NM_000397.4:c.496G>A MANE Select	NP_000388.2:p.Gly166Ser