Canonical Allele Identifier: CA2693426433
Gene: CYBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795938_37795939insGTA , CM000685.2:g.37795938_37795939insGTA GRCh38
NC_000023.10:g.37655191_37655192insGTA , CM000685.1:g.37655191_37655192insGTA GRCh37
NC_000023.9:g.37540131_37540132insGTA NCBI36
NG_009065.1:g.20918_20919insGTA , LRG_53:g.20918_20919insGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-13_338-12insGTA ENSP00000512461.1:n.338-13_338-12insGTA
ENST00000696171.1:c.388-13_388-12insGTA ENSP00000512462.1:n.388-13_388-12insGTA
ENST00000696172.1:c.338-3017_338-3016insGTA ENSP00000512463.1:n.338-3017_338-3016insGTA
ENST00000378588.5:c.484-13_484-12insGTA MANE Select ENSP00000367851.4:n.484-13_484-12insGTA
ENST00000378588.4:c.484-13_484-12insGTA ENSP00000367851.4:n.484-13_484-12insGTA
ENST00000465127.1:c.171+369938_171+369939insGTA ENSP00000417050.1:n.171+369938_171+369939insGTA
NM_000397.3:c.484-13_484-12insGTA , LRG_53t1:c.484-13_484-12insGTA NP_000388.2:n.484-13_484-12insGTA
XM_011543890.1:c.178-13_178-12insGTA XP_011542192.1:n.178-13_178-12insGTA
NM_000397.4:c.484-13_484-12insGTA MANE Select NP_000388.2:n.484-13_484-12insGTA