Canonical Allele Identifier: CA641363610

Gene: CYBB

Linked Data

• dbSNP Id: rs1569479385
• gnomAD v2: X-37655142-C-CGT
• gnomAD v3: X-37795889-C-CGT
• gnomAD v4: X-37795889-C-CGT
• MyVariant Identifiers: chrX:g.37655143_37655158delinsGTATGTGTGTGTGTGTGT (hg19) ; chrX:g.37795890_37795905delinsGTATGTGTGTGTGTGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795889_37795890insGT , CM000685.2:g.37795889_37795890insGT	GRCh38
NC_000023.10:g.37655142_37655143insGT , CM000685.1:g.37655142_37655143insGT	GRCh37
NC_000023.9:g.37540082_37540083insGT	NCBI36
NG_009065.1:g.20869_20870insGT , LRG_53:g.20869_20870insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-62_338-61insGT	ENSP00000512461.1:n.338-62_338-61insGT
ENST00000696171.1:c.388-62_388-61insGT	ENSP00000512462.1:n.388-62_388-61insGT
ENST00000696172.1:c.338-3066_338-3065insGT	ENSP00000512463.1:n.338-3066_338-3065insGT
ENST00000378588.5:c.484-62_484-61insGT MANE Select	ENSP00000367851.4:n.484-62_484-61insGT
ENST00000378588.4:c.484-62_484-61insGT	ENSP00000367851.4:n.484-62_484-61insGT
ENST00000465127.1:c.171+369889_171+369890insGT	ENSP00000417050.1:n.171+369889_171+369890insGT
NM_000397.3:c.484-62_484-61insGT , LRG_53t1:c.484-62_484-61insGT	NP_000388.2:n.484-62_484-61insGT
XM_011543890.1:c.178-62_178-61insGT	XP_011542192.1:n.178-62_178-61insGT
NM_000397.4:c.484-62_484-61insGT MANE Select	NP_000388.2:n.484-62_484-61insGT