Canonical Allele Identifier: CA2424683059
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804277T= , CM000685.2:g.37804277T= GRCh38
NC_000023.10:g.37663530T= , CM000685.1:g.37663530T= GRCh37
NC_000023.9:g.37548474T= NCBI36
NG_009065.1:g.29261T= , LRG_53:g.29261T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*660+147T= ENSP00000512461.1:n.*660+147T=
ENST00000696171.1:c.1055+147T= ENSP00000512462.1:n.1055+147T=
ENST00000378588.5:c.1151+147T= MANE Select ENSP00000367851.4:n.1151+147T=
ENST00000378588.4:c.1151+147T= ENSP00000367851.4:n.1151+147T=
ENST00000465127.1:c.171+378277T= ENSP00000417050.1:n.171+378277T=
NM_000397.3:c.1151+147T= , LRG_53t1:c.1151+147T= NP_000388.2:n.1151+147T=
XM_011543890.1:c.845+147T= XP_011542192.1:n.845+147T=
NM_000397.4:c.1151+147T= MANE Select NP_000388.2:n.1151+147T=