Canonical Allele Identifier: CA8228425
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs776204307

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88647222_88647262del , CM000678.2:g.88647222_88647262del GRCh38
NC_000016.9:g.88713630_88713670del , CM000678.1:g.88713630_88713670del GRCh37
NC_000016.8:g.87241131_87241171del NCBI36
NG_007291.1:g.8796_8836del , LRG_52:g.8796_8836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.129-79_129-39del ENSP00000455537.2:n.129-79_129-39del
ENST00000696156.1:c.129-79_129-39del ENSP00000512446.1:n.129-79_129-39del
ENST00000696157.1:c.129-79_129-39del ENSP00000512447.1:n.129-79_129-39del
ENST00000696158.1:c.129-79_129-39del ENSP00000512448.1:n.129-79_129-39del
ENST00000696159.1:c.129-79_129-39del ENSP00000512449.1:n.129-79_129-39del
ENST00000696160.1:c.129-79_129-39del ENSP00000512450.1:n.129-79_129-39del
ENST00000696161.1:c.129-79_129-39del ENSP00000512451.1:n.129-79_129-39del
ENST00000696162.1:c.129-79_129-39del ENSP00000512452.1:n.129-79_129-39del
ENST00000696163.1:c.129-79_129-39del ENSP00000512453.1:n.129-79_129-39del
ENST00000261623.8:c.129-79_129-39del MANE Select ENSP00000261623.3:n.129-79_129-39del
ENST00000261623.7:c.129-79_129-39del ENSP00000261623.3:n.129-79_129-39del
ENST00000562209.1:n.147-79_147-39del
ENST00000563526.5:n.104-79_104-39del
ENST00000566229.1:c.118-79_118-39del ENSP00000457060.1:n.118-79_118-39del
ENST00000566534.5:n.151-79_151-39del
ENST00000567174.5:c.129-79_129-39del ENSP00000454951.1:n.129-79_129-39del
ENST00000568278.1:c.129-79_129-39del ENSP00000455506.1:n.129-79_129-39del
ENST00000569359.5:c.129-79_129-39del ENSP00000456079.1:n.129-79_129-39del
NM_000101.3:c.129-79_129-39del NP_000092.2:n.129-79_129-39del
XM_011522905.1:c.129-79_129-39del XP_011521207.1:n.129-79_129-39del
XM_011522905.3:c.129-79_129-39del XP_011521207.1:n.129-79_129-39del
NM_000101.4:c.129-79_129-39del MANE Select NP_000092.2:n.129-79_129-39del