Canonical Allele Identifier: CA875141427
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1238574247
MyVariant Identifiers: chrX:g.37783912del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783914del , CM000685.2:g.37783914del GRCh38
NC_000023.10:g.37643167del , CM000685.1:g.37643167del GRCh37
NC_000023.9:g.37528111del NCBI36
NG_009065.1:g.8898del , LRG_53:g.8898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+314del ENSP00000512461.1:n.252+314del
ENST00000696171.1:c.156+314del ENSP00000512462.1:n.156+314del
ENST00000696172.1:c.252+314del ENSP00000512463.1:n.252+314del
ENST00000696173.1:n.260+314del
ENST00000378588.5:c.252+314del MANE Select ENSP00000367851.4:n.252+314del
ENST00000378588.4:c.252+314del ENSP00000367851.4:n.252+314del
ENST00000465127.1:c.171+357914del ENSP00000417050.1:n.171+357914del
NM_000397.3:c.252+314del , LRG_53t1:c.252+314del NP_000388.2:n.252+314del
XM_011543890.1:c.-179+314del XP_011542192.1:n.-179+314del
NM_000397.4:c.252+314del MANE Select NP_000388.2:n.252+314del