Canonical Allele Identifier: CA412977266

Gene: CYBB

Linked Data

• MyVariant Identifiers: chrX:g.37663242G>C (hg19) ; chrX:g.37803989G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37803989G>C , CM000685.2:g.37803989G>C	GRCh38
NC_000023.10:g.37663242G>C , CM000685.1:g.37663242G>C	GRCh37
NC_000023.9:g.37548186G>C	NCBI36
NG_009065.1:g.28973G>C , LRG_53:g.28973G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696170.1:c.*519G>C	ENSP00000512461.1:n.*519G>C
ENST00000696171.1:c.914G>C	ENSP00000512462.1:p.Trp305Ser
ENST00000378588.5:c.1010G>C MANE Select	ENSP00000367851.4:p.Trp337Ser
ENST00000378588.4:c.1010G>C	ENSP00000367851.4:p.Trp337Ser
ENST00000465127.1:c.171+377989G>C	ENSP00000417050.1:n.171+377989G>C
ENST00000492288.1:n.435G>C
NM_000397.3:c.1010G>C , LRG_53t1:c.1010G>C	NP_000388.2:p.Trp337Ser
XM_011543890.1:c.704G>C	XP_011542192.1:p.Trp235Ser
NM_000397.4:c.1010G>C MANE Select	NP_000388.2:p.Trp337Ser