Canonical Allele Identifier: CA10383751

Gene: CYBB

Linked Data

• dbSNP Id: rs782779261
• ExAC: X:37655197 T / A
• gnomAD v2: X-37655197-T-A
• gnomAD v4: X-37795944-T-A
• MyVariant Identifiers: chrX:g.37655197T>A (hg19) ; chrX:g.37795944T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795944T>A , CM000685.2:g.37795944T>A	GRCh38
NC_000023.10:g.37655197T>A , CM000685.1:g.37655197T>A	GRCh37
NC_000023.9:g.37540137T>A	NCBI36
NG_009065.1:g.20924T>A , LRG_53:g.20924T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.338-7T>A	ENSP00000512461.1:n.338-7T>A
ENST00000696171.1:c.388-7T>A	ENSP00000512462.1:n.388-7T>A
ENST00000696172.1:c.338-3011T>A	ENSP00000512463.1:n.338-3011T>A
ENST00000378588.5:c.484-7T>A MANE Select	ENSP00000367851.4:n.484-7T>A
ENST00000378588.4:c.484-7T>A	ENSP00000367851.4:n.484-7T>A
ENST00000465127.1:c.171+369944T>A	ENSP00000417050.1:n.171+369944T>A
NM_000397.3:c.484-7T>A , LRG_53t1:c.484-7T>A	NP_000388.2:n.484-7T>A
XM_011543890.1:c.178-7T>A	XP_011542192.1:n.178-7T>A
NM_000397.4:c.484-7T>A MANE Select	NP_000388.2:n.484-7T>A