Canonical Allele Identifier: CA515673985
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37803882-C-A
MyVariant Identifiers: chrX:g.37663135C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803882C>A , CM000685.2:g.37803882C>A GRCh38
NC_000023.10:g.37663135C>A , CM000685.1:g.37663135C>A GRCh37
NC_000023.9:g.37548079C>A NCBI36
NG_009065.1:g.28866C>A , LRG_53:g.28866C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*412C>A ENSP00000512461.1:n.*412C>A
ENST00000696171.1:c.807C>A ENSP00000512462.1:p.Val269=
ENST00000378588.5:c.903C>A MANE Select ENSP00000367851.4:p.Val301=
ENST00000378588.4:c.903C>A ENSP00000367851.4:p.Val301=
ENST00000465127.1:c.171+377882C>A ENSP00000417050.1:n.171+377882C>A
ENST00000492288.1:n.328C>A
NM_000397.3:c.903C>A , LRG_53t1:c.903C>A NP_000388.2:p.Val301=
XM_011543890.1:c.597C>A XP_011542192.1:p.Val199=
NM_000397.4:c.903C>A MANE Select NP_000388.2:p.Val301=
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