Canonical Allele Identifier: CA2424682899
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1929494274

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803686C>T , CM000685.2:g.37803686C>T GRCh38
NC_000023.10:g.37662939C>T , CM000685.1:g.37662939C>T GRCh37
NC_000023.9:g.37547883C>T NCBI36
NG_009065.1:g.28670C>T , LRG_53:g.28670C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*407-191C>T ENSP00000512461.1:n.*407-191C>T
ENST00000696171.1:c.802-191C>T ENSP00000512462.1:n.802-191C>T
ENST00000378588.5:c.898-191C>T MANE Select ENSP00000367851.4:n.898-191C>T
ENST00000378588.4:c.898-191C>T ENSP00000367851.4:n.898-191C>T
ENST00000465127.1:c.171+377686C>T ENSP00000417050.1:n.171+377686C>T
ENST00000492288.1:n.323-191C>T
NM_000397.3:c.898-191C>T , LRG_53t1:c.898-191C>T NP_000388.2:n.898-191C>T
XM_011543890.1:c.592-191C>T XP_011542192.1:n.592-191C>T
NM_000397.4:c.898-191C>T MANE Select NP_000388.2:n.898-191C>T