Canonical Allele Identifier: CA2738411304
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs2146811538

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795897del , CM000685.2:g.37795897del GRCh38
NC_000023.10:g.37655150del , CM000685.1:g.37655150del GRCh37
NC_000023.9:g.37540090del NCBI36
NG_009065.1:g.20877del , LRG_53:g.20877del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-54del ENSP00000512461.1:n.338-54del
ENST00000696171.1:c.388-54del ENSP00000512462.1:n.388-54del
ENST00000696172.1:c.338-3058del ENSP00000512463.1:n.338-3058del
ENST00000378588.5:c.484-54del MANE Select ENSP00000367851.4:n.484-54del
ENST00000378588.4:c.484-54del ENSP00000367851.4:n.484-54del
ENST00000465127.1:c.171+369897del ENSP00000417050.1:n.171+369897del
NM_000397.3:c.484-54del , LRG_53t1:c.484-54del NP_000388.2:n.484-54del
XM_011543890.1:c.178-54del XP_011542192.1:n.178-54del
NM_000397.4:c.484-54del MANE Select NP_000388.2:n.484-54del