Canonical Allele Identifier: CA412976085

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655291A>G (hg19) ; chrX:g.37796038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796038A>G , CM000685.2:g.37796038A>G	GRCh38
NC_000023.10:g.37655291A>G , CM000685.1:g.37655291A>G	GRCh37
NC_000023.9:g.37540231A>G	NCBI36
NG_009065.1:g.21018A>G , LRG_53:g.21018A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*80A>G	ENSP00000512461.1:n.*80A>G
ENST00000696171.1:c.475A>G	ENSP00000512462.1:p.Thr159Ala
ENST00000696172.1:c.338-2917A>G	ENSP00000512463.1:n.338-2917A>G
ENST00000378588.5:c.571A>G MANE Select	ENSP00000367851.4:p.Thr191Ala
ENST00000378588.4:c.571A>G	ENSP00000367851.4:p.Thr191Ala
ENST00000465127.1:c.171+370038A>G	ENSP00000417050.1:n.171+370038A>G
NM_000397.3:c.571A>G , LRG_53t1:c.571A>G	NP_000388.2:p.Thr191Ala
XM_011543890.1:c.265A>G	XP_011542192.1:p.Thr89Ala
NM_000397.4:c.571A>G MANE Select	NP_000388.2:p.Thr191Ala