Canonical Allele Identifier: CA641363622

Gene: CYBB

Linked Data

• gnomAD v2: X-37655191-T-TGTG
• gnomAD v3: X-37795938-T-TGTG
• gnomAD v4: X-37795938-T-TGTG
• MyVariant Identifiers: chrX:g.37655191_37655192insGTG (hg19) ; chrX:g.37795938_37795939insGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795938_37795939insGTG , CM000685.2:g.37795938_37795939insGTG	GRCh38
NC_000023.10:g.37655191_37655192insGTG , CM000685.1:g.37655191_37655192insGTG	GRCh37
NC_000023.9:g.37540131_37540132insGTG	NCBI36
NG_009065.1:g.20918_20919insGTG , LRG_53:g.20918_20919insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-13_338-12insGTG	ENSP00000512461.1:n.338-13_338-12insGTG
ENST00000696171.1:c.388-13_388-12insGTG	ENSP00000512462.1:n.388-13_388-12insGTG
ENST00000696172.1:c.338-3017_338-3016insGTG	ENSP00000512463.1:n.338-3017_338-3016insGTG
ENST00000378588.5:c.484-13_484-12insGTG MANE Select	ENSP00000367851.4:n.484-13_484-12insGTG
ENST00000378588.4:c.484-13_484-12insGTG	ENSP00000367851.4:n.484-13_484-12insGTG
ENST00000465127.1:c.171+369938_171+369939insGTG	ENSP00000417050.1:n.171+369938_171+369939insGTG
NM_000397.3:c.484-13_484-12insGTG , LRG_53t1:c.484-13_484-12insGTG	NP_000388.2:n.484-13_484-12insGTG
XM_011543890.1:c.178-13_178-12insGTG	XP_011542192.1:n.178-13_178-12insGTG
NM_000397.4:c.484-13_484-12insGTG MANE Select	NP_000388.2:n.484-13_484-12insGTG