Canonical Allele Identifier: CA980332324

Gene: CYBA

Linked Data

• dbSNP Id: rs1907144106
• gnomAD v3: 16-88643299-G-GCT
• gnomAD v4: 16-88643299-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643300_88643301dup , CM000678.2:g.88643300_88643301dup	GRCh38
NC_000016.9:g.88709708_88709709dup , CM000678.1:g.88709708_88709709dup	GRCh37
NC_000016.8:g.87237209_87237210dup	NCBI36
NG_007291.1:g.12749_12750dup , LRG_52:g.12749_12750dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*52_*53dup	ENSP00000512446.1:n.*52_*53dup
ENST00000696157.1:c.*857_*858dup	ENSP00000512447.1:n.*857_*858dup
ENST00000696158.1:c.*894_*895dup	ENSP00000512448.1:n.*894_*895dup
ENST00000696159.1:c.*563_*564dup	ENSP00000512449.1:n.*563_*564dup
ENST00000696160.1:c.*52_*53dup	ENSP00000512450.1:n.*52_*53dup
ENST00000696161.1:c.*5_*6dup	ENSP00000512451.1:n.*5_*6dup
ENST00000696162.1:c.*1359_*1360dup	ENSP00000512452.1:n.*1359_*1360dup
ENST00000696163.1:c.*52_*53dup	ENSP00000512453.1:n.*52_*53dup
ENST00000261623.8:c.*52_*53dup MANE Select	ENSP00000261623.3:n.*52_*53dup
ENST00000261623.7:c.*52_*53dup	ENSP00000261623.3:n.*52_*53dup
NM_000101.3:c.*52_*53dup	NP_000092.2:n.*52_*53dup
NM_000101.4:c.*52_*53dup MANE Select	NP_000092.2:n.*52_*53dup