Canonical Allele Identifier: CA2241201218

Gene: CYBA

Linked Data

• dbSNP Id: rs1907267581
• gnomAD v4: 16-88646105-G-GCGCCACTCACCAGTAGGTAGATGC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88646109_88646132dup , CM000678.2:g.88646109_88646132dup	GRCh38
NC_000016.9:g.88712517_88712540dup , CM000678.1:g.88712517_88712540dup	GRCh37
NC_000016.8:g.87240018_87240041dup	NCBI36
NG_007291.1:g.9921_9944dup , LRG_52:g.9921_9944dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000565588.6:c.356_369+10dup
ENST00000696156.1:c.272_285+10dup
ENST00000696157.1:c.356_369+10dup
ENST00000696158.1:c.356_369+10dup
ENST00000696159.1:c.356_369+10dup
ENST00000696160.1:c.356_369+10dup
ENST00000696161.1:c.486_499+10dup
ENST00000696162.1:c.356_369+10dup
ENST00000696163.1:c.305_318+10dup
ENST00000261623.8:c.356_369+10dup
ENST00000261623.7:c.356_369+10dup
ENST00000563526.5:n.888_911dup
ENST00000565588.5:c.140_153+10dup
ENST00000566229.1:c.345_358+10dup
ENST00000566534.5:n.935_948+10dup
ENST00000567174.5:c.356_369+10dup
ENST00000569359.5:c.356_379dup	ENSP00000456079.1:p.Gly126_Ala127insGlyIl...
NM_000101.3:c.356_369+10dup
XM_011522905.1:c.356_369+10dup
XM_011522905.3:c.356_369+10dup
NM_000101.4:c.356_369+10dup