Canonical Allele Identifier: CA515670892

Gene: CYBB

Linked Data

• gnomAD v4: X-37796022-C-T
• MyVariant Identifiers: chrX:g.37655275C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796022C>T , CM000685.2:g.37796022C>T	GRCh38
NC_000023.10:g.37655275C>T , CM000685.1:g.37655275C>T	GRCh37
NC_000023.9:g.37540215C>T	NCBI36
NG_009065.1:g.21002C>T , LRG_53:g.21002C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*64C>T	ENSP00000512461.1:n.*64C>T
ENST00000696171.1:c.459C>T	ENSP00000512462.1:p.Cys153=
ENST00000696172.1:c.338-2933C>T	ENSP00000512463.1:n.338-2933C>T
ENST00000378588.5:c.555C>T MANE Select	ENSP00000367851.4:p.Cys185=
ENST00000378588.4:c.555C>T	ENSP00000367851.4:p.Cys185=
ENST00000465127.1:c.171+370022C>T	ENSP00000417050.1:n.171+370022C>T
NM_000397.3:c.555C>T , LRG_53t1:c.555C>T	NP_000388.2:p.Cys185=
XM_011543890.1:c.249C>T	XP_011542192.1:p.Cys83=
NM_000397.4:c.555C>T MANE Select	NP_000388.2:p.Cys185=