Canonical Allele Identifier: CA515671500

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37655368C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37796115C>T , CM000685.2:g.37796115C>T	GRCh38
NC_000023.10:g.37655368C>T , CM000685.1:g.37655368C>T	GRCh37
NC_000023.9:g.37540308C>T	NCBI36
NG_009065.1:g.21095C>T , LRG_53:g.21095C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*157C>T	ENSP00000512461.1:n.*157C>T
ENST00000696171.1:c.552C>T	ENSP00000512462.1:p.Phe184=
ENST00000696172.1:c.338-2840C>T	ENSP00000512463.1:n.338-2840C>T
ENST00000378588.5:c.648C>T MANE Select	ENSP00000367851.4:p.Phe216=
ENST00000378588.4:c.648C>T	ENSP00000367851.4:p.Phe216=
ENST00000465127.1:c.171+370115C>T	ENSP00000417050.1:n.171+370115C>T
NM_000397.3:c.648C>T , LRG_53t1:c.648C>T	NP_000388.2:p.Phe216=
XM_011543890.1:c.342C>T	XP_011542192.1:p.Phe114=
NM_000397.4:c.648C>T MANE Select	NP_000388.2:p.Phe216=