Canonical Allele Identifier: CA412975772

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655212A>T (hg19) ; chrX:g.37795959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795959A>T , CM000685.2:g.37795959A>T	GRCh38
NC_000023.10:g.37655212A>T , CM000685.1:g.37655212A>T	GRCh37
NC_000023.9:g.37540152A>T	NCBI36
NG_009065.1:g.20939A>T , LRG_53:g.20939A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*1A>T	ENSP00000512461.1:n.*1A>T
ENST00000696171.1:c.396A>T	ENSP00000512462.1:p.Glu132Asp
ENST00000696172.1:c.338-2996A>T	ENSP00000512463.1:n.338-2996A>T
ENST00000378588.5:c.492A>T MANE Select	ENSP00000367851.4:p.Glu164Asp
ENST00000378588.4:c.492A>T	ENSP00000367851.4:p.Glu164Asp
ENST00000465127.1:c.171+369959A>T	ENSP00000417050.1:n.171+369959A>T
NM_000397.3:c.492A>T , LRG_53t1:c.492A>T	NP_000388.2:p.Glu164Asp
XM_011543890.1:c.186A>T	XP_011542192.1:p.Glu62Asp
NM_000397.4:c.492A>T MANE Select	NP_000388.2:p.Glu164Asp