Canonical Allele Identifier: CA2424680359
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795923T= , CM000685.2:g.37795923T= GRCh38
NC_000023.10:g.37655176T= , CM000685.1:g.37655176T= GRCh37
NC_000023.9:g.37540116T= NCBI36
NG_009065.1:g.20903T= , LRG_53:g.20903T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-28T= ENSP00000512461.1:n.338-28T=
ENST00000696171.1:c.388-28T= ENSP00000512462.1:n.388-28T=
ENST00000696172.1:c.338-3032T= ENSP00000512463.1:n.338-3032T=
ENST00000378588.5:c.484-28T= MANE Select ENSP00000367851.4:n.484-28T=
ENST00000378588.4:c.484-28T= ENSP00000367851.4:n.484-28T=
ENST00000465127.1:c.171+369923T= ENSP00000417050.1:n.171+369923T=
NM_000397.3:c.484-28T= , LRG_53t1:c.484-28T= NP_000388.2:n.484-28T=
XM_011543890.1:c.178-28T= XP_011542192.1:n.178-28T=
NM_000397.4:c.484-28T= MANE Select NP_000388.2:n.484-28T=