Canonical Allele Identifier: CA2424676074
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37782132_37782134delinsCCG , CM000685.2:g.37782132_37782134delinsCCG GRCh38
NC_000023.10:g.37641385_37641387delinsCCG , CM000685.1:g.37641385_37641387delinsCCG GRCh37
NC_000023.9:g.37526329_37526331delinsCCG NCBI36
NG_009065.1:g.7116_7118delinsCCG , LRG_53:g.7116_7118delinsCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.90_92delinsCCG ENSP00000512461.1:p.Tyr30=
ENST00000696171.1:c.46-1358_46-1356delinsCCG ENSP00000512462.1:n.46-1358_46-1356delinsCCG
ENST00000696172.1:c.90_92delinsCCG ENSP00000512463.1:p.Tyr30=
ENST00000696173.1:n.98_100delinsCCG
ENST00000378588.5:c.90_92delinsCCG MANE Select ENSP00000367851.4:p.Tyr30=
ENST00000378588.4:c.90_92delinsCCG ENSP00000367851.4:p.Tyr30=
ENST00000465127.1:c.171+356132_171+356134delinsCCG ENSP00000417050.1:n.171+356132_171+356134delinsCCG
NM_000397.3:c.90_92delinsCCG , LRG_53t1:c.90_92delinsCCG NP_000388.2:p.Tyr30=
XM_011543890.1:c.-341_-339delinsCCG XP_011542192.1:n.-341_-339delinsCCG
NM_000397.4:c.90_92delinsCCG MANE Select NP_000388.2:p.Tyr30=