Canonical Allele Identifier: CA2424676665
Gene: CYBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783931A= , CM000685.2:g.37783931A= GRCh38
NC_000023.10:g.37643184A= , CM000685.1:g.37643184A= GRCh37
NC_000023.9:g.37528128A= NCBI36
NG_009065.1:g.8915A= , LRG_53:g.8915A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+331A= ENSP00000512461.1:n.252+331A=
ENST00000696171.1:c.156+331A= ENSP00000512462.1:n.156+331A=
ENST00000696172.1:c.252+331A= ENSP00000512463.1:n.252+331A=
ENST00000696173.1:n.260+331A=
ENST00000378588.5:c.252+331A= MANE Select ENSP00000367851.4:n.252+331A=
ENST00000378588.4:c.252+331A= ENSP00000367851.4:n.252+331A=
ENST00000465127.1:c.171+357931A= ENSP00000417050.1:n.171+357931A=
NM_000397.3:c.252+331A= , LRG_53t1:c.252+331A= NP_000388.2:n.252+331A=
XM_011543890.1:c.-179+331A= XP_011542192.1:n.-179+331A=
NM_000397.4:c.252+331A= MANE Select NP_000388.2:n.252+331A=
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