Canonical Allele Identifier: CA2634847719

Gene: CYBA

Linked Data

• gnomAD v4: 16-88643329-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643332del , CM000678.2:g.88643332del	GRCh38
NC_000016.9:g.88709740del , CM000678.1:g.88709740del	GRCh37
NC_000016.8:g.87237241del	NCBI36
NG_007291.1:g.12720del , LRG_52:g.12720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*23del	ENSP00000512446.1:n.*23del
ENST00000696157.1:c.*828del	ENSP00000512447.1:n.*828del
ENST00000696158.1:c.*865del	ENSP00000512448.1:n.*865del
ENST00000696159.1:c.*534del	ENSP00000512449.1:n.*534del
ENST00000696160.1:c.*23del	ENSP00000512450.1:n.*23del
ENST00000696161.1:c.741del	ENSP00000512451.1:p.Ala248ProfsTer?
ENST00000696162.1:c.*1330del	ENSP00000512452.1:n.*1330del
ENST00000696163.1:c.*23del	ENSP00000512453.1:n.*23del
ENST00000261623.8:c.*23del MANE Select	ENSP00000261623.3:n.*23del
ENST00000261623.7:c.*23del	ENSP00000261623.3:n.*23del
NM_000101.3:c.*23del	NP_000092.2:n.*23del
NM_000101.4:c.*23del MANE Select	NP_000092.2:n.*23del