Canonical Allele Identifier: CA2424682920
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1929495649

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803760G>A , CM000685.2:g.37803760G>A GRCh38
NC_000023.10:g.37663013G>A , CM000685.1:g.37663013G>A GRCh37
NC_000023.9:g.37547957G>A NCBI36
NG_009065.1:g.28744G>A , LRG_53:g.28744G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*407-117G>A ENSP00000512461.1:n.*407-117G>A
ENST00000696171.1:c.802-117G>A ENSP00000512462.1:n.802-117G>A
ENST00000378588.5:c.898-117G>A MANE Select ENSP00000367851.4:n.898-117G>A
ENST00000378588.4:c.898-117G>A ENSP00000367851.4:n.898-117G>A
ENST00000465127.1:c.171+377760G>A ENSP00000417050.1:n.171+377760G>A
ENST00000492288.1:n.323-117G>A
NM_000397.3:c.898-117G>A , LRG_53t1:c.898-117G>A NP_000388.2:n.898-117G>A
XM_011543890.1:c.592-117G>A XP_011542192.1:n.592-117G>A
NM_000397.4:c.898-117G>A MANE Select NP_000388.2:n.898-117G>A