Canonical Allele Identifier: CA412975940
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796003G>C , CM000685.2:g.37796003G>C GRCh38
NC_000023.10:g.37655256G>C , CM000685.1:g.37655256G>C GRCh37
NC_000023.9:g.37540196G>C NCBI36
NG_009065.1:g.20983G>C , LRG_53:g.20983G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*45G>C ENSP00000512461.1:n.*45G>C
ENST00000696171.1:c.440G>C ENSP00000512462.1:p.Gly147Ala
ENST00000696172.1:c.338-2952G>C ENSP00000512463.1:n.338-2952G>C
ENST00000378588.5:c.536G>C MANE Select ENSP00000367851.4:p.Gly179Ala
ENST00000378588.4:c.536G>C ENSP00000367851.4:p.Gly179Ala
ENST00000465127.1:c.171+370003G>C ENSP00000417050.1:n.171+370003G>C
NM_000397.3:c.536G>C , LRG_53t1:c.536G>C NP_000388.2:p.Gly179Ala
XM_011543890.1:c.230G>C XP_011542192.1:p.Gly77Ala
NM_000397.4:c.536G>C MANE Select NP_000388.2:p.Gly179Ala