Canonical Allele Identifier: CA2424676641

Gene: CYBB

Linked Data

• dbSNP Id: rs1160952893

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783886_37783887del , CM000685.2:g.37783886_37783887del	GRCh38
NC_000023.10:g.37643139_37643140del , CM000685.1:g.37643139_37643140del	GRCh37
NC_000023.9:g.37528083_37528084del	NCBI36
NG_009065.1:g.8870_8871del , LRG_53:g.8870_8871del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+286_252+287del	ENSP00000512461.1:n.252+286_252+287del
ENST00000696171.1:c.156+286_156+287del	ENSP00000512462.1:n.156+286_156+287del
ENST00000696172.1:c.252+286_252+287del	ENSP00000512463.1:n.252+286_252+287del
ENST00000696173.1:n.260+286_260+287del
ENST00000378588.5:c.252+286_252+287del MANE Select	ENSP00000367851.4:n.252+286_252+287del
ENST00000378588.4:c.252+286_252+287del	ENSP00000367851.4:n.252+286_252+287del
ENST00000465127.1:c.171+357886_171+357887del	ENSP00000417050.1:n.171+357886_171+357887del
NM_000397.3:c.252+286_252+287del , LRG_53t1:c.252+286_252+287del	NP_000388.2:n.252+286_252+287del
XM_011543890.1:c.-179+286_-179+287del	XP_011542192.1:n.-179+286_-179+287del
NM_000397.4:c.252+286_252+287del MANE Select	NP_000388.2:n.252+286_252+287del