Canonical Allele Identifier: CA875138887
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1348792079
gnomAD v4: X-37804941-G-A
MyVariant Identifiers: chrX:g.37804941G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804941G>A , CM000685.2:g.37804941G>A GRCh38
NC_000023.10:g.37664194G>A , CM000685.1:g.37664194G>A GRCh37
NC_000023.9:g.37549138G>A NCBI36
NG_009065.1:g.29925G>A , LRG_53:g.29925G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*661-65G>A ENSP00000512461.1:n.*661-65G>A
ENST00000696171.1:c.1056-65G>A ENSP00000512462.1:n.1056-65G>A
ENST00000378588.5:c.1152-65G>A MANE Select ENSP00000367851.4:n.1152-65G>A
ENST00000378588.4:c.1152-65G>A ENSP00000367851.4:n.1152-65G>A
ENST00000465127.1:c.171+378941G>A ENSP00000417050.1:n.171+378941G>A
NM_000397.3:c.1152-65G>A , LRG_53t1:c.1152-65G>A NP_000388.2:n.1152-65G>A
XM_011543890.1:c.846-65G>A XP_011542192.1:n.846-65G>A
NM_000397.4:c.1152-65G>A MANE Select NP_000388.2:n.1152-65G>A
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