Canonical Allele Identifier: CA515671599

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655389A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796136A>T , CM000685.2:g.37796136A>T	GRCh38
NC_000023.10:g.37655389A>T , CM000685.1:g.37655389A>T	GRCh37
NC_000023.9:g.37540329A>T	NCBI36
NG_009065.1:g.21116A>T , LRG_53:g.21116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*178A>T	ENSP00000512461.1:n.*178A>T
ENST00000696171.1:c.573A>T	ENSP00000512462.1:p.Gly191=
ENST00000696172.1:c.338-2819A>T	ENSP00000512463.1:n.338-2819A>T
ENST00000378588.5:c.669A>T MANE Select	ENSP00000367851.4:p.Gly223=
ENST00000378588.4:c.669A>T	ENSP00000367851.4:p.Gly223=
ENST00000465127.1:c.171+370136A>T	ENSP00000417050.1:n.171+370136A>T
NM_000397.3:c.669A>T , LRG_53t1:c.669A>T	NP_000388.2:p.Gly223=
XM_011543890.1:c.363A>T	XP_011542192.1:p.Gly121=
NM_000397.4:c.669A>T MANE Select	NP_000388.2:p.Gly223=