Canonical Allele Identifier: CA515671550

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655374C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796121C>T , CM000685.2:g.37796121C>T	GRCh38
NC_000023.10:g.37655374C>T , CM000685.1:g.37655374C>T	GRCh37
NC_000023.9:g.37540314C>T	NCBI36
NG_009065.1:g.21101C>T , LRG_53:g.21101C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*163C>T	ENSP00000512461.1:n.*163C>T
ENST00000696171.1:c.558C>T	ENSP00000512462.1:p.Gly186=
ENST00000696172.1:c.338-2834C>T	ENSP00000512463.1:n.338-2834C>T
ENST00000378588.5:c.654C>T MANE Select	ENSP00000367851.4:p.Gly218=
ENST00000378588.4:c.654C>T	ENSP00000367851.4:p.Gly218=
ENST00000465127.1:c.171+370121C>T	ENSP00000417050.1:n.171+370121C>T
NM_000397.3:c.654C>T , LRG_53t1:c.654C>T	NP_000388.2:p.Gly218=
XM_011543890.1:c.348C>T	XP_011542192.1:p.Gly116=
NM_000397.4:c.654C>T MANE Select	NP_000388.2:p.Gly218=