Canonical Allele Identifier: CA641363586

Gene: CYBB

Linked Data

• dbSNP Id: rs1556468437
• gnomAD v2: X-37655437-A-G
• gnomAD v4: X-37796184-A-G
• MyVariant Identifiers: chrX:g.37655437A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796184A>G , CM000685.2:g.37796184A>G	GRCh38
NC_000023.10:g.37655437A>G , CM000685.1:g.37655437A>G	GRCh37
NC_000023.9:g.37540377A>G	NCBI36
NG_009065.1:g.21164A>G , LRG_53:g.21164A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*183+43A>G	ENSP00000512461.1:n.*183+43A>G
ENST00000696171.1:c.578+43A>G	ENSP00000512462.1:n.578+43A>G
ENST00000696172.1:c.338-2771A>G	ENSP00000512463.1:n.338-2771A>G
ENST00000378588.5:c.674+43A>G MANE Select	ENSP00000367851.4:n.674+43A>G
ENST00000378588.4:c.674+43A>G	ENSP00000367851.4:n.674+43A>G
ENST00000465127.1:c.171+370184A>G	ENSP00000417050.1:n.171+370184A>G
NM_000397.3:c.674+43A>G , LRG_53t1:c.674+43A>G	NP_000388.2:n.674+43A>G
XM_011543890.1:c.368+43A>G	XP_011542192.1:n.368+43A>G
NM_000397.4:c.674+43A>G MANE Select	NP_000388.2:n.674+43A>G