Canonical Allele Identifier: CA2241201749
Gene: CYBA HGNC NCBI

Linked Data

dbSNP Id: rs1907309818

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88646942del , CM000678.2:g.88646942del GRCh38
NC_000016.9:g.88713350del , CM000678.1:g.88713350del GRCh37
NC_000016.8:g.87240851del NCBI36
NG_007291.1:g.9110del , LRG_52:g.9110del

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.204-102del ENSP00000455537.2:n.204-102del
ENST00000696156.1:c.203+161del ENSP00000512446.1:n.203+161del
ENST00000696157.1:c.204-102del ENSP00000512447.1:n.204-102del
ENST00000696158.1:c.204-102del ENSP00000512448.1:n.204-102del
ENST00000696159.1:c.204-102del ENSP00000512449.1:n.204-102del
ENST00000696160.1:c.204-102del ENSP00000512450.1:n.204-102del
ENST00000696161.1:c.232del ENSP00000512451.1:p.Glu78ArgfsTer?
ENST00000696162.1:c.204-102del ENSP00000512452.1:n.204-102del
ENST00000696163.1:c.204-153del ENSP00000512453.1:n.204-153del
ENST00000261623.8:c.204-102del MANE Select ENSP00000261623.3:n.204-102del
ENST00000261623.7:c.204-102del ENSP00000261623.3:n.204-102del
ENST00000562209.1:n.382del
ENST00000563526.5:n.179-102del
ENST00000566229.1:c.193-102del ENSP00000457060.1:n.193-102del
ENST00000566534.5:n.226-102del
ENST00000567174.5:c.204-102del ENSP00000454951.1:n.204-102del
ENST00000568278.1:c.204-102del ENSP00000455506.1:n.204-102del
ENST00000569359.5:c.204-102del ENSP00000456079.1:n.204-102del
NM_000101.3:c.204-102del NP_000092.2:n.204-102del
XM_011522905.1:c.204-102del XP_011521207.1:n.204-102del
XM_011522905.3:c.204-102del XP_011521207.1:n.204-102del
NM_000101.4:c.204-102del MANE Select NP_000092.2:n.204-102del