Canonical Allele Identifier: CA2693426429
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795937_37795938insGTGTGTGTGTGTG , CM000685.2:g.37795937_37795938insGTGTGTGTGTGTG GRCh38
NC_000023.10:g.37655190_37655191insGTGTGTGTGTGTG , CM000685.1:g.37655190_37655191insGTGTGTGTGTGTG GRCh37
NC_000023.9:g.37540130_37540131insGTGTGTGTGTGTG NCBI36
NG_009065.1:g.20917_20918insGTGTGTGTGTGTG , LRG_53:g.20917_20918insGTGTGTGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-14_338-13insGTGTGTGTGTGTG ENSP00000512461.1:n.338-14_338-13insGTGTGTGTGTGTG
ENST00000696171.1:c.388-14_388-13insGTGTGTGTGTGTG ENSP00000512462.1:n.388-14_388-13insGTGTGTGTGTGTG
ENST00000696172.1:c.338-3018_338-3017insGTGTGTGTGTGTG ENSP00000512463.1:n.338-3018_338-3017insGTGTGTGTGTGTG
ENST00000378588.5:c.484-14_484-13insGTGTGTGTGTGTG MANE Select ENSP00000367851.4:n.484-14_484-13insGTGTGTGTGTGTG
ENST00000378588.4:c.484-14_484-13insGTGTGTGTGTGTG ENSP00000367851.4:n.484-14_484-13insGTGTGTGTGTGTG
ENST00000465127.1:c.171+369937_171+369938insGTGTGTGTGTGTG ENSP00000417050.1:n.171+369937_171+369938insGTGTGTGTGTGTG
NM_000397.3:c.484-14_484-13insGTGTGTGTGTGTG , LRG_53t1:c.484-14_484-13insGTGTGTGTGTGTG NP_000388.2:n.484-14_484-13insGTGTGTGTGTGTG
XM_011543890.1:c.178-14_178-13insGTGTGTGTGTGTG XP_011542192.1:n.178-14_178-13insGTGTGTGTGTGTG
NM_000397.4:c.484-14_484-13insGTGTGTGTGTGTG MANE Select NP_000388.2:n.484-14_484-13insGTGTGTGTGTGTG