Canonical Allele Identifier: CA2693426381

Gene: CYBB

Linked Data

• gnomAD v4: X-37795894-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795895_37795896insAT , CM000685.2:g.37795895_37795896insAT	GRCh38
NC_000023.10:g.37655148_37655149insAT , CM000685.1:g.37655148_37655149insAT	GRCh37
NC_000023.9:g.37540088_37540089insAT	NCBI36
NG_009065.1:g.20875_20876insAT , LRG_53:g.20875_20876insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-56_338-55insAT	ENSP00000512461.1:n.338-56_338-55insAT
ENST00000696171.1:c.388-56_388-55insAT	ENSP00000512462.1:n.388-56_388-55insAT
ENST00000696172.1:c.338-3060_338-3059insAT	ENSP00000512463.1:n.338-3060_338-3059insAT
ENST00000378588.5:c.484-56_484-55insAT MANE Select	ENSP00000367851.4:n.484-56_484-55insAT
ENST00000378588.4:c.484-56_484-55insAT	ENSP00000367851.4:n.484-56_484-55insAT
ENST00000465127.1:c.171+369895_171+369896insAT	ENSP00000417050.1:n.171+369895_171+369896insAT
NM_000397.3:c.484-56_484-55insAT , LRG_53t1:c.484-56_484-55insAT	NP_000388.2:n.484-56_484-55insAT
XM_011543890.1:c.178-56_178-55insAT	XP_011542192.1:n.178-56_178-55insAT
NM_000397.4:c.484-56_484-55insAT MANE Select	NP_000388.2:n.484-56_484-55insAT