Canonical Allele Identifier: CA412977762

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664329G>C (hg19) ; chrX:g.37805076G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805076G>C , CM000685.2:g.37805076G>C	GRCh38
NC_000023.10:g.37664329G>C , CM000685.1:g.37664329G>C	GRCh37
NC_000023.9:g.37549273G>C	NCBI36
NG_009065.1:g.30060G>C , LRG_53:g.30060G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*731G>C	ENSP00000512461.1:n.*731G>C
ENST00000696171.1:c.1126G>C	ENSP00000512462.1:p.Gly376Arg
ENST00000378588.5:c.1222G>C MANE Select	ENSP00000367851.4:p.Gly408Arg
ENST00000378588.4:c.1222G>C	ENSP00000367851.4:p.Gly408Arg
ENST00000465127.1:c.171+379076G>C	ENSP00000417050.1:n.171+379076G>C
NM_000397.3:c.1222G>C , LRG_53t1:c.1222G>C	NP_000388.2:p.Gly408Arg
XM_011543890.1:c.916G>C	XP_011542192.1:p.Gly306Arg
NM_000397.4:c.1222G>C MANE Select	NP_000388.2:p.Gly408Arg