Canonical Allele Identifier: CA2695232421
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37782134_37782135insC , CM000685.2:g.37782134_37782135insC GRCh38
NC_000023.10:g.37641387_37641388insC , CM000685.1:g.37641387_37641388insC GRCh37
NC_000023.9:g.37526331_37526332insC NCBI36
NG_009065.1:g.7118_7119insC , LRG_53:g.7118_7119insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.92_93insC ENSP00000512461.1:p.Val32GlyfsTer3
ENST00000696171.1:c.46-1356_46-1355insC ENSP00000512462.1:n.46-1356_46-1355insC
ENST00000696172.1:c.92_93insC ENSP00000512463.1:p.Val32GlyfsTer3
ENST00000696173.1:n.100_101insC
ENST00000378588.5:c.92_93insC MANE Select ENSP00000367851.4:p.Val32GlyfsTer3
ENST00000378588.4:c.92_93insC ENSP00000367851.4:p.Val32GlyfsTer3
ENST00000465127.1:c.171+356134_171+356135insC ENSP00000417050.1:n.171+356134_171+356135insC
NM_000397.3:c.92_93insC , LRG_53t1:c.92_93insC NP_000388.2:p.Val32GlyfsTer3
XM_011543890.1:c.-339_-338insC XP_011542192.1:n.-339_-338insC
NM_000397.4:c.92_93insC MANE Select NP_000388.2:p.Val32GlyfsTer3