Canonical Allele Identifier: CA10383744

Gene: CYBB

Linked Data

• dbSNP Id: rs1556468303
• ExAC: X:37655190 T / TGTGTGTGTG
• gnomAD v2: X-37655190-T-TGTGTGTGTG
• gnomAD v4: X-37795937-T-TGTGTGTGTG
• MyVariant Identifiers: chrX:g.37655190_37655191insGTGTGTGTG (hg19) ; chrX:g.37795937_37795938insGTGTGTGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795937_37795938insGTGTGTGTG , CM000685.2:g.37795937_37795938insGTGTGTGTG	GRCh38
NC_000023.10:g.37655190_37655191insGTGTGTGTG , CM000685.1:g.37655190_37655191insGTGTGTGTG	GRCh37
NC_000023.9:g.37540130_37540131insGTGTGTGTG	NCBI36
NG_009065.1:g.20917_20918insGTGTGTGTG , LRG_53:g.20917_20918insGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-14_338-13insGTGTGTGTG	ENSP00000512461.1:n.338-14_338-13insGTGTGTGTG
ENST00000696171.1:c.388-14_388-13insGTGTGTGTG	ENSP00000512462.1:n.388-14_388-13insGTGTGTGTG
ENST00000696172.1:c.338-3018_338-3017insGTGTGTGTG	ENSP00000512463.1:n.338-3018_338-3017insGTGTGTGTG
ENST00000378588.5:c.484-14_484-13insGTGTGTGTG MANE Select	ENSP00000367851.4:n.484-14_484-13insGTGTGTGTG
ENST00000378588.4:c.484-14_484-13insGTGTGTGTG	ENSP00000367851.4:n.484-14_484-13insGTGTGTGTG
ENST00000465127.1:c.171+369937_171+369938insGTGTGTGTG	ENSP00000417050.1:n.171+369937_171+369938insGTGTGTGTG
NM_000397.3:c.484-14_484-13insGTGTGTGTG , LRG_53t1:c.484-14_484-13insGTGTGTGTG	NP_000388.2:n.484-14_484-13insGTGTGTGTG
XM_011543890.1:c.178-14_178-13insGTGTGTGTG	XP_011542192.1:n.178-14_178-13insGTGTGTGTG
NM_000397.4:c.484-14_484-13insGTGTGTGTG MANE Select	NP_000388.2:n.484-14_484-13insGTGTGTGTG