Canonical Allele Identifier: CA2579582977

Gene: CYBB

Linked Data

• gnomAD v4: X-37795929-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795930_37795931insCG , CM000685.2:g.37795930_37795931insCG	GRCh38
NC_000023.10:g.37655183_37655184insCG , CM000685.1:g.37655183_37655184insCG	GRCh37
NC_000023.9:g.37540123_37540124insCG	NCBI36
NG_009065.1:g.20910_20911insCG , LRG_53:g.20910_20911insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-21_338-20insCG	ENSP00000512461.1:n.338-21_338-20insCG
ENST00000696171.1:c.388-21_388-20insCG	ENSP00000512462.1:n.388-21_388-20insCG
ENST00000696172.1:c.338-3025_338-3024insCG	ENSP00000512463.1:n.338-3025_338-3024insCG
ENST00000378588.5:c.484-21_484-20insCG MANE Select	ENSP00000367851.4:n.484-21_484-20insCG
ENST00000378588.4:c.484-21_484-20insCG	ENSP00000367851.4:n.484-21_484-20insCG
ENST00000465127.1:c.171+369930_171+369931insCG	ENSP00000417050.1:n.171+369930_171+369931insCG
NM_000397.3:c.484-21_484-20insCG , LRG_53t1:c.484-21_484-20insCG	NP_000388.2:n.484-21_484-20insCG
XM_011543890.1:c.178-21_178-20insCG	XP_011542192.1:n.178-21_178-20insCG
NM_000397.4:c.484-21_484-20insCG MANE Select	NP_000388.2:n.484-21_484-20insCG