Canonical Allele Identifier: CA412976369
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796102T>G , CM000685.2:g.37796102T>G GRCh38
NC_000023.10:g.37655355T>G , CM000685.1:g.37655355T>G GRCh37
NC_000023.9:g.37540295T>G NCBI36
NG_009065.1:g.21082T>G , LRG_53:g.21082T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*144T>G ENSP00000512461.1:n.*144T>G
ENST00000696171.1:c.539T>G ENSP00000512462.1:p.Phe180Cys
ENST00000696172.1:c.338-2853T>G ENSP00000512463.1:n.338-2853T>G
ENST00000378588.5:c.635T>G MANE Select ENSP00000367851.4:p.Phe212Cys
ENST00000378588.4:c.635T>G ENSP00000367851.4:p.Phe212Cys
ENST00000465127.1:c.171+370102T>G ENSP00000417050.1:n.171+370102T>G
NM_000397.3:c.635T>G , LRG_53t1:c.635T>G NP_000388.2:p.Phe212Cys
XM_011543890.1:c.329T>G XP_011542192.1:p.Phe110Cys
NM_000397.4:c.635T>G MANE Select NP_000388.2:p.Phe212Cys