Canonical Allele Identifier: CA2424680387
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795975G= , CM000685.2:g.37795975G= GRCh38
NC_000023.10:g.37655228G= , CM000685.1:g.37655228G= GRCh37
NC_000023.9:g.37540168G= NCBI36
NG_009065.1:g.20955G= , LRG_53:g.20955G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*17G= ENSP00000512461.1:n.*17G=
ENST00000696171.1:c.412G= ENSP00000512462.1:p.Ala138=
ENST00000696172.1:c.338-2980G= ENSP00000512463.1:n.338-2980G=
ENST00000378588.5:c.508G= MANE Select ENSP00000367851.4:p.Ala170=
ENST00000378588.4:c.508G= ENSP00000367851.4:p.Ala170=
ENST00000465127.1:c.171+369975G= ENSP00000417050.1:n.171+369975G=
NM_000397.3:c.508G= , LRG_53t1:c.508G= NP_000388.2:p.Ala170=
XM_011543890.1:c.202G= XP_011542192.1:p.Ala68=
NM_000397.4:c.508G= MANE Select NP_000388.2:p.Ala170=