Canonical Allele Identifier: CA412977019

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37663136A>C (hg19) ; chrX:g.37803883A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803883A>C , CM000685.2:g.37803883A>C	GRCh38
NC_000023.10:g.37663136A>C , CM000685.1:g.37663136A>C	GRCh37
NC_000023.9:g.37548080A>C	NCBI36
NG_009065.1:g.28867A>C , LRG_53:g.28867A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696170.1:c.*413A>C	ENSP00000512461.1:n.*413A>C
ENST00000696171.1:c.808A>C	ENSP00000512462.1:p.Thr270Pro
ENST00000378588.5:c.904A>C MANE Select	ENSP00000367851.4:p.Thr302Pro
ENST00000378588.4:c.904A>C	ENSP00000367851.4:p.Thr302Pro
ENST00000465127.1:c.171+377883A>C	ENSP00000417050.1:n.171+377883A>C
ENST00000492288.1:n.329A>C
NM_000397.3:c.904A>C , LRG_53t1:c.904A>C	NP_000388.2:p.Thr302Pro
XM_011543890.1:c.598A>C	XP_011542192.1:p.Thr200Pro
NM_000397.4:c.904A>C MANE Select	NP_000388.2:p.Thr302Pro