Canonical Allele Identifier: CA2579582820
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37803785-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803785G>T , CM000685.2:g.37803785G>T GRCh38
NC_000023.10:g.37663038G>T , CM000685.1:g.37663038G>T GRCh37
NC_000023.9:g.37547982G>T NCBI36
NG_009065.1:g.28769G>T , LRG_53:g.28769G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*407-92G>T ENSP00000512461.1:n.*407-92G>T
ENST00000696171.1:c.802-92G>T ENSP00000512462.1:n.802-92G>T
ENST00000378588.5:c.898-92G>T MANE Select ENSP00000367851.4:n.898-92G>T
ENST00000378588.4:c.898-92G>T ENSP00000367851.4:n.898-92G>T
ENST00000465127.1:c.171+377785G>T ENSP00000417050.1:n.171+377785G>T
ENST00000492288.1:n.323-92G>T
NM_000397.3:c.898-92G>T , LRG_53t1:c.898-92G>T NP_000388.2:n.898-92G>T
XM_011543890.1:c.592-92G>T XP_011542192.1:n.592-92G>T
NM_000397.4:c.898-92G>T MANE Select NP_000388.2:n.898-92G>T