Canonical Allele Identifier: CA412976207

Gene: CYBB

Linked Data

• ClinVar Variation Id: 450884
• ClinVar RCV Id: RCV000518911
• dbSNP Id: rs1556468360
• MyVariant Identifiers: chrX:g.37655319C>T (hg19) ; chrX:g.37796066C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796066C>T , CM000685.2:g.37796066C>T	GRCh38
NC_000023.10:g.37655319C>T , CM000685.1:g.37655319C>T	GRCh37
NC_000023.9:g.37540259C>T	NCBI36
NG_009065.1:g.21046C>T , LRG_53:g.21046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*108C>T	ENSP00000512461.1:n.*108C>T
ENST00000696171.1:c.503C>T	ENSP00000512462.1:p.Ser168Phe
ENST00000696172.1:c.338-2889C>T	ENSP00000512463.1:n.338-2889C>T
ENST00000378588.5:c.599C>T MANE Select	ENSP00000367851.4:p.Ser200Phe
ENST00000378588.4:c.599C>T	ENSP00000367851.4:p.Ser200Phe
ENST00000465127.1:c.171+370066C>T	ENSP00000417050.1:n.171+370066C>T
NM_000397.3:c.599C>T , LRG_53t1:c.599C>T	NP_000388.2:p.Ser200Phe
XM_011543890.1:c.293C>T	XP_011542192.1:p.Ser98Phe
NM_000397.4:c.599C>T MANE Select	NP_000388.2:p.Ser200Phe