Canonical Allele Identifier: CA412975910
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795996A>T , CM000685.2:g.37795996A>T GRCh38
NC_000023.10:g.37655249A>T , CM000685.1:g.37655249A>T GRCh37
NC_000023.9:g.37540189A>T NCBI36
NG_009065.1:g.20976A>T , LRG_53:g.20976A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*38A>T ENSP00000512461.1:n.*38A>T
ENST00000696171.1:c.433A>T ENSP00000512462.1:p.Ile145Phe
ENST00000696172.1:c.338-2959A>T ENSP00000512463.1:n.338-2959A>T
ENST00000378588.5:c.529A>T MANE Select ENSP00000367851.4:p.Ile177Phe
ENST00000378588.4:c.529A>T ENSP00000367851.4:p.Ile177Phe
ENST00000465127.1:c.171+369996A>T ENSP00000417050.1:n.171+369996A>T
NM_000397.3:c.529A>T , LRG_53t1:c.529A>T NP_000388.2:p.Ile177Phe
XM_011543890.1:c.223A>T XP_011542192.1:p.Ile75Phe
NM_000397.4:c.529A>T MANE Select NP_000388.2:p.Ile177Phe