Canonical Allele Identifier: CA412976339
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796095C>T , CM000685.2:g.37796095C>T GRCh38
NC_000023.10:g.37655348C>T , CM000685.1:g.37655348C>T GRCh37
NC_000023.9:g.37540288C>T NCBI36
NG_009065.1:g.21075C>T , LRG_53:g.21075C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*137C>T ENSP00000512461.1:n.*137C>T
ENST00000696171.1:c.532C>T ENSP00000512462.1:p.His178Tyr
ENST00000696172.1:c.338-2860C>T ENSP00000512463.1:n.338-2860C>T
ENST00000378588.5:c.628C>T MANE Select ENSP00000367851.4:p.His210Tyr
ENST00000378588.4:c.628C>T ENSP00000367851.4:p.His210Tyr
ENST00000465127.1:c.171+370095C>T ENSP00000417050.1:n.171+370095C>T
NM_000397.3:c.628C>T , LRG_53t1:c.628C>T NP_000388.2:p.His210Tyr
XM_011543890.1:c.322C>T XP_011542192.1:p.His108Tyr
NM_000397.4:c.628C>T MANE Select NP_000388.2:p.His210Tyr