Canonical Allele Identifier: CA2693426421

Gene: CYBB

Linked Data

• gnomAD v4: X-37795933-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795934del , CM000685.2:g.37795934del	GRCh38
NC_000023.10:g.37655187del , CM000685.1:g.37655187del	GRCh37
NC_000023.9:g.37540127del	NCBI36
NG_009065.1:g.20914del , LRG_53:g.20914del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-17del	ENSP00000512461.1:n.338-17del
ENST00000696171.1:c.388-17del	ENSP00000512462.1:n.388-17del
ENST00000696172.1:c.338-3021del	ENSP00000512463.1:n.338-3021del
ENST00000378588.5:c.484-17del MANE Select	ENSP00000367851.4:n.484-17del
ENST00000378588.4:c.484-17del	ENSP00000367851.4:n.484-17del
ENST00000465127.1:c.171+369934del	ENSP00000417050.1:n.171+369934del
NM_000397.3:c.484-17del , LRG_53t1:c.484-17del	NP_000388.2:n.484-17del
XM_011543890.1:c.178-17del	XP_011542192.1:n.178-17del
NM_000397.4:c.484-17del MANE Select	NP_000388.2:n.484-17del