Canonical Allele Identifier: CA412972896

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37642841G>T (hg19) ; chrX:g.37783588G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37783588G>T , CM000685.2:g.37783588G>T	GRCh38
NC_000023.10:g.37642841G>T , CM000685.1:g.37642841G>T	GRCh37
NC_000023.9:g.37527785G>T	NCBI36
NG_009065.1:g.8572G>T , LRG_53:g.8572G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.240G>T	ENSP00000512461.1:p.Arg80Ser
ENST00000696171.1:c.144G>T	ENSP00000512462.1:p.Arg48Ser
ENST00000696172.1:c.240G>T	ENSP00000512463.1:p.Arg80Ser
ENST00000696173.1:n.248G>T
ENST00000378588.5:c.240G>T MANE Select	ENSP00000367851.4:p.Arg80Ser
ENST00000378588.4:c.240G>T	ENSP00000367851.4:p.Arg80Ser
ENST00000465127.1:c.171+357588G>T	ENSP00000417050.1:n.171+357588G>T
NM_000397.3:c.240G>T , LRG_53t1:c.240G>T	NP_000388.2:p.Arg80Ser
XM_011543890.1:c.-191G>T	XP_011542192.1:n.-191G>T
NM_000397.4:c.240G>T MANE Select	NP_000388.2:p.Arg80Ser