Canonical Allele Identifier: CA515677320
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37805021-G-A
MyVariant Identifiers: chrX:g.37664274G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37805021G>A , CM000685.2:g.37805021G>A GRCh38
NC_000023.10:g.37664274G>A , CM000685.1:g.37664274G>A GRCh37
NC_000023.9:g.37549218G>A NCBI36
NG_009065.1:g.30005G>A , LRG_53:g.30005G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*676G>A ENSP00000512461.1:n.*676G>A
ENST00000696171.1:c.1071G>A ENSP00000512462.1:p.Gly357=
ENST00000378588.5:c.1167G>A MANE Select ENSP00000367851.4:p.Gly389=
ENST00000378588.4:c.1167G>A ENSP00000367851.4:p.Gly389=
ENST00000465127.1:c.171+379021G>A ENSP00000417050.1:n.171+379021G>A
NM_000397.3:c.1167G>A , LRG_53t1:c.1167G>A NP_000388.2:p.Gly389=
XM_011543890.1:c.861G>A XP_011542192.1:p.Gly287=
NM_000397.4:c.1167G>A MANE Select NP_000388.2:p.Gly389=
Search 100 bp 5'
Search 100 bp 3'