Canonical Allele Identifier: CA2695233053
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795943T>G , CM000685.2:g.37795943T>G GRCh38
NC_000023.10:g.37655196T>G , CM000685.1:g.37655196T>G GRCh37
NC_000023.9:g.37540136T>G NCBI36
NG_009065.1:g.20923T>G , LRG_53:g.20923T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-8T>G ENSP00000512461.1:n.338-8T>G
ENST00000696171.1:c.388-8T>G ENSP00000512462.1:n.388-8T>G
ENST00000696172.1:c.338-3012T>G ENSP00000512463.1:n.338-3012T>G
ENST00000378588.5:c.484-8T>G MANE Select ENSP00000367851.4:n.484-8T>G
ENST00000378588.4:c.484-8T>G ENSP00000367851.4:n.484-8T>G
ENST00000465127.1:c.171+369943T>G ENSP00000417050.1:n.171+369943T>G
NM_000397.3:c.484-8T>G , LRG_53t1:c.484-8T>G NP_000388.2:n.484-8T>G
XM_011543890.1:c.178-8T>G XP_011542192.1:n.178-8T>G
NM_000397.4:c.484-8T>G MANE Select NP_000388.2:n.484-8T>G