Canonical Allele Identifier: CA640896434
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1556470884
MyVariant Identifiers: chrX:g.37663425del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804176del , CM000685.2:g.37804176del GRCh38
NC_000023.10:g.37663429del , CM000685.1:g.37663429del GRCh37
NC_000023.9:g.37548373del NCBI36
NG_009065.1:g.29160del , LRG_53:g.29160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*660+46del ENSP00000512461.1:n.*660+46del
ENST00000696171.1:c.1055+46del ENSP00000512462.1:n.1055+46del
ENST00000378588.5:c.1151+46del MANE Select ENSP00000367851.4:n.1151+46del
ENST00000378588.4:c.1151+46del ENSP00000367851.4:n.1151+46del
ENST00000465127.1:c.171+378176del ENSP00000417050.1:n.171+378176del
NM_000397.3:c.1151+46del , LRG_53t1:c.1151+46del NP_000388.2:n.1151+46del
XM_011543890.1:c.845+46del XP_011542192.1:n.845+46del
NM_000397.4:c.1151+46del MANE Select NP_000388.2:n.1151+46del