Canonical Allele Identifier: CA875141401

Gene: CYBB

Linked Data

• dbSNP Id: rs1433717824
• gnomAD v3: X-37783874-A-G
• gnomAD v4: X-37783874-A-G
• MyVariant Identifiers: chrX:g.37783874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783874A>G , CM000685.2:g.37783874A>G	GRCh38
NC_000023.10:g.37643127A>G , CM000685.1:g.37643127A>G	GRCh37
NC_000023.9:g.37528071A>G	NCBI36
NG_009065.1:g.8858A>G , LRG_53:g.8858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.252+274A>G	ENSP00000512461.1:n.252+274A>G
ENST00000696171.1:c.156+274A>G	ENSP00000512462.1:n.156+274A>G
ENST00000696172.1:c.252+274A>G	ENSP00000512463.1:n.252+274A>G
ENST00000696173.1:n.260+274A>G
ENST00000378588.5:c.252+274A>G MANE Select	ENSP00000367851.4:n.252+274A>G
ENST00000378588.4:c.252+274A>G	ENSP00000367851.4:n.252+274A>G
ENST00000465127.1:c.171+357874A>G	ENSP00000417050.1:n.171+357874A>G
NM_000397.3:c.252+274A>G , LRG_53t1:c.252+274A>G	NP_000388.2:n.252+274A>G
XM_011543890.1:c.-179+274A>G	XP_011542192.1:n.-179+274A>G
NM_000397.4:c.252+274A>G MANE Select	NP_000388.2:n.252+274A>G