Canonical Allele Identifier: CA2634847727

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643333-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643335_88643336del , CM000678.2:g.88643335_88643336del	GRCh38
NC_000016.9:g.88709743_88709744del , CM000678.1:g.88709743_88709744del	GRCh37
NC_000016.8:g.87237244_87237245del	NCBI36
NG_007291.1:g.12715_12716del , LRG_52:g.12715_12716del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696156.1:c.*18_*19del	ENSP00000512446.1:n.*18_*19del
ENST00000696157.1:c.*823_*824del	ENSP00000512447.1:n.*823_*824del
ENST00000696158.1:c.*860_*861del	ENSP00000512448.1:n.*860_*861del
ENST00000696159.1:c.*529_*530del	ENSP00000512449.1:n.*529_*530del
ENST00000696160.1:c.*18_*19del	ENSP00000512450.1:n.*18_*19del
ENST00000696161.1:c.736_737del	ENSP00000512451.1:p.Pro246SerfsTer?
ENST00000696162.1:c.*1325_*1326del	ENSP00000512452.1:n.*1325_*1326del
ENST00000696163.1:c.*18_*19del	ENSP00000512453.1:n.*18_*19del
ENST00000261623.8:c.*18_*19del MANE Select	ENSP00000261623.3:n.*18_*19del
ENST00000261623.7:c.*18_*19del	ENSP00000261623.3:n.*18_*19del
NM_000101.3:c.*18_*19del	NP_000092.2:n.*18_*19del
NM_000101.4:c.*18_*19del MANE Select	NP_000092.2:n.*18_*19del