Canonical Allele Identifier: CA916081862
Gene: CYBA HGNC NCBI

Linked Data

ClinVar Variation Id: 845152
ClinVar RCV Id: RCV001048168

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643538_88647000del , CM000678.2:g.88643538_88647000del GRCh38
NC_000016.9:g.88709946_88713408del , CM000678.1:g.88709946_88713408del GRCh37
NC_000016.8:g.87237447_87240909del NCBI36
NG_007291.1:g.9051_12513del , LRG_52:g.9051_12513del

Transcript Alleles

HGVS Amino-acid change
ENST00000565588.6:c.203+102_414del
ENST00000696156.1:c.203+102_320del
ENST00000696157.1:c.203+102_*621del
ENST00000696158.1:c.203+102_*658del
ENST00000696159.1:c.203+102_*327del
ENST00000696160.1:c.203+102_431del
ENST00000696161.1:c.204-31_534del
ENST00000696162.1:c.203+102_*1123del
ENST00000696163.1:c.203+102_353del
ENST00000261623.8:c.203+102_404del
ENST00000261623.7:c.203+102_404del
ENST00000566534.5:n.225+102_983del
NM_000101.3:c.203+102_404del
NM_000101.4:c.203+102_404del