Canonical Allele Identifier: CA875133372

Gene: CYBB

Linked Data

• dbSNP Id: rs782505530
• gnomAD v3: X-37795898-G-GTA
• gnomAD v4: X-37795898-G-GTA
• MyVariant Identifiers: chrX:g.37655151_37655152insTA (hg19) ; chrX:g.37795898_37795899insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795899_37795900insAT , CM000685.2:g.37795899_37795900insAT	GRCh38
NC_000023.10:g.37655152_37655153insAT , CM000685.1:g.37655152_37655153insAT	GRCh37
NC_000023.9:g.37540092_37540093insAT	NCBI36
NG_009065.1:g.20879_20880insAT , LRG_53:g.20879_20880insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-52_338-51insAT	ENSP00000512461.1:n.338-52_338-51insAT
ENST00000696171.1:c.388-52_388-51insAT	ENSP00000512462.1:n.388-52_388-51insAT
ENST00000696172.1:c.338-3056_338-3055insAT	ENSP00000512463.1:n.338-3056_338-3055insAT
ENST00000378588.5:c.484-52_484-51insAT MANE Select	ENSP00000367851.4:n.484-52_484-51insAT
ENST00000378588.4:c.484-52_484-51insAT	ENSP00000367851.4:n.484-52_484-51insAT
ENST00000465127.1:c.171+369899_171+369900insAT	ENSP00000417050.1:n.171+369899_171+369900insAT
NM_000397.3:c.484-52_484-51insAT , LRG_53t1:c.484-52_484-51insAT	NP_000388.2:n.484-52_484-51insAT
XM_011543890.1:c.178-52_178-51insAT	XP_011542192.1:n.178-52_178-51insAT
NM_000397.4:c.484-52_484-51insAT MANE Select	NP_000388.2:n.484-52_484-51insAT