Canonical Allele Identifier: CA515671127

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655312C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796059C>A , CM000685.2:g.37796059C>A	GRCh38
NC_000023.10:g.37655312C>A , CM000685.1:g.37655312C>A	GRCh37
NC_000023.9:g.37540252C>A	NCBI36
NG_009065.1:g.21039C>A , LRG_53:g.21039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*101C>A	ENSP00000512461.1:n.*101C>A
ENST00000696171.1:c.496C>A	ENSP00000512462.1:p.Arg166=
ENST00000696172.1:c.338-2896C>A	ENSP00000512463.1:n.338-2896C>A
ENST00000378588.5:c.592C>A MANE Select	ENSP00000367851.4:p.Arg198=
ENST00000378588.4:c.592C>A	ENSP00000367851.4:p.Arg198=
ENST00000465127.1:c.171+370059C>A	ENSP00000417050.1:n.171+370059C>A
NM_000397.3:c.592C>A , LRG_53t1:c.592C>A	NP_000388.2:p.Arg198=
XM_011543890.1:c.286C>A	XP_011542192.1:p.Arg96=
NM_000397.4:c.592C>A MANE Select	NP_000388.2:p.Arg198=