Canonical Allele Identifier: CA412977780

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37664339T>C (hg19) ; chrX:g.37805086T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37805086T>C , CM000685.2:g.37805086T>C	GRCh38
NC_000023.10:g.37664339T>C , CM000685.1:g.37664339T>C	GRCh37
NC_000023.9:g.37549283T>C	NCBI36
NG_009065.1:g.30070T>C , LRG_53:g.30070T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*741T>C	ENSP00000512461.1:n.*741T>C
ENST00000696171.1:c.1136T>C	ENSP00000512462.1:p.Ile379Thr
ENST00000378588.5:c.1232T>C MANE Select	ENSP00000367851.4:p.Ile411Thr
ENST00000378588.4:c.1232T>C	ENSP00000367851.4:p.Ile411Thr
ENST00000465127.1:c.171+379086T>C	ENSP00000417050.1:n.171+379086T>C
NM_000397.3:c.1232T>C , LRG_53t1:c.1232T>C	NP_000388.2:p.Ile411Thr
XM_011543890.1:c.926T>C	XP_011542192.1:p.Ile309Thr
NM_000397.4:c.1232T>C MANE Select	NP_000388.2:p.Ile411Thr