Canonical Allele Identifier: CA2695232443
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783543dup , CM000685.2:g.37783543dup GRCh38
NC_000023.10:g.37642796dup , CM000685.1:g.37642796dup GRCh37
NC_000023.9:g.37527740dup NCBI36
NG_009065.1:g.8527dup , LRG_53:g.8527dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.195dup ENSP00000512461.1:p.Leu66AlafsTer?
ENST00000696171.1:c.99dup ENSP00000512462.1:p.Leu34AlafsTer?
ENST00000696172.1:c.195dup ENSP00000512463.1:p.Leu66AlafsTer?
ENST00000696173.1:n.203dup
ENST00000378588.5:c.195dup MANE Select ENSP00000367851.4:p.Leu66AlafsTer?
ENST00000378588.4:c.195dup ENSP00000367851.4:p.Leu66AlafsTer?
ENST00000465127.1:c.171+357543dup ENSP00000417050.1:n.171+357543dup
NM_000397.3:c.195dup , LRG_53t1:c.195dup NP_000388.2:p.Leu66AlafsTer?
XM_011543890.1:c.-236dup XP_011542192.1:n.-236dup
NM_000397.4:c.195dup MANE Select NP_000388.2:p.Leu66AlafsTer?