Canonical Allele Identifier: CA2424680374
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1929295483

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795935_37795936insTT , CM000685.2:g.37795935_37795936insTT GRCh38
NC_000023.10:g.37655188_37655189insTT , CM000685.1:g.37655188_37655189insTT GRCh37
NC_000023.9:g.37540128_37540129insTT NCBI36
NG_009065.1:g.20915_20916insTT , LRG_53:g.20915_20916insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-16_338-15insTT ENSP00000512461.1:n.338-16_338-15insTT
ENST00000696171.1:c.388-16_388-15insTT ENSP00000512462.1:n.388-16_388-15insTT
ENST00000696172.1:c.338-3020_338-3019insTT ENSP00000512463.1:n.338-3020_338-3019insTT
ENST00000378588.5:c.484-16_484-15insTT MANE Select ENSP00000367851.4:n.484-16_484-15insTT
ENST00000378588.4:c.484-16_484-15insTT ENSP00000367851.4:n.484-16_484-15insTT
ENST00000465127.1:c.171+369935_171+369936insTT ENSP00000417050.1:n.171+369935_171+369936insTT
NM_000397.3:c.484-16_484-15insTT , LRG_53t1:c.484-16_484-15insTT NP_000388.2:n.484-16_484-15insTT
XM_011543890.1:c.178-16_178-15insTT XP_011542192.1:n.178-16_178-15insTT
NM_000397.4:c.484-16_484-15insTT MANE Select NP_000388.2:n.484-16_484-15insTT