Canonical Allele Identifier: CA412975907
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*38A>C ENSP00000512461.1:n.*38A>C
ENST00000696171.1:c.433A>C ENSP00000512462.1:p.Ile145Leu
ENST00000696172.1:c.338-2959A>C ENSP00000512463.1:n.338-2959A>C
ENST00000378588.5:c.529A>C MANE Select ENSP00000367851.4:p.Ile177Leu
ENST00000378588.4:c.529A>C ENSP00000367851.4:p.Ile177Leu
ENST00000465127.1:c.171+369996A>C ENSP00000417050.1:n.171+369996A>C
NM_000397.3:c.529A>C , LRG_53t1:c.529A>C NP_000388.2:p.Ile177Leu
XM_011543890.1:c.223A>C XP_011542192.1:p.Ile75Leu
NM_000397.4:c.529A>C MANE Select NP_000388.2:p.Ile177Leu