Canonical Allele Identifier: CA412977357
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37663283T>A (hg19) chrX:g.37804030T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804030T>A , CM000685.2:g.37804030T>A GRCh38
NC_000023.10:g.37663283T>A , CM000685.1:g.37663283T>A GRCh37
NC_000023.9:g.37548227T>A NCBI36
NG_009065.1:g.29014T>A , LRG_53:g.29014T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*560T>A ENSP00000512461.1:n.*560T>A
ENST00000696171.1:c.955T>A ENSP00000512462.1:p.Phe319Ile
ENST00000378588.5:c.1051T>A MANE Select ENSP00000367851.4:p.Phe351Ile
ENST00000378588.4:c.1051T>A ENSP00000367851.4:p.Phe351Ile
ENST00000465127.1:c.171+378030T>A ENSP00000417050.1:n.171+378030T>A
ENST00000492288.1:n.476T>A
NM_000397.3:c.1051T>A , LRG_53t1:c.1051T>A NP_000388.2:p.Phe351Ile
XM_011543890.1:c.745T>A XP_011542192.1:p.Phe249Ile
NM_000397.4:c.1051T>A MANE Select NP_000388.2:p.Phe351Ile
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