Canonical Allele Identifier: CA515670839

Gene: CYBB

Linked Data

• gnomAD v4: X-37795983-C-G
• MyVariant Identifiers: chrX:g.37655236C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37795983C>G , CM000685.2:g.37795983C>G	GRCh38
NC_000023.10:g.37655236C>G , CM000685.1:g.37655236C>G	GRCh37
NC_000023.9:g.37540176C>G	NCBI36
NG_009065.1:g.20963C>G , LRG_53:g.20963C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*25C>G	ENSP00000512461.1:n.*25C>G
ENST00000696171.1:c.420C>G	ENSP00000512462.1:p.Thr140=
ENST00000696172.1:c.338-2972C>G	ENSP00000512463.1:n.338-2972C>G
ENST00000378588.5:c.516C>G MANE Select	ENSP00000367851.4:p.Thr172=
ENST00000378588.4:c.516C>G	ENSP00000367851.4:p.Thr172=
ENST00000465127.1:c.171+369983C>G	ENSP00000417050.1:n.171+369983C>G
NM_000397.3:c.516C>G , LRG_53t1:c.516C>G	NP_000388.2:p.Thr172=
XM_011543890.1:c.210C>G	XP_011542192.1:p.Thr70=
NM_000397.4:c.516C>G MANE Select	NP_000388.2:p.Thr172=