Canonical Allele Identifier: CA2693426682
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37804854-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804854A>T , CM000685.2:g.37804854A>T GRCh38
NC_000023.10:g.37664107A>T , CM000685.1:g.37664107A>T GRCh37
NC_000023.9:g.37549051A>T NCBI36
NG_009065.1:g.29838A>T , LRG_53:g.29838A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*661-152A>T ENSP00000512461.1:n.*661-152A>T
ENST00000696171.1:c.1056-152A>T ENSP00000512462.1:n.1056-152A>T
ENST00000378588.5:c.1152-152A>T MANE Select ENSP00000367851.4:n.1152-152A>T
ENST00000378588.4:c.1152-152A>T ENSP00000367851.4:n.1152-152A>T
ENST00000465127.1:c.171+378854A>T ENSP00000417050.1:n.171+378854A>T
NM_000397.3:c.1152-152A>T , LRG_53t1:c.1152-152A>T NP_000388.2:n.1152-152A>T
XM_011543890.1:c.846-152A>T XP_011542192.1:n.846-152A>T
NM_000397.4:c.1152-152A>T MANE Select NP_000388.2:n.1152-152A>T
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