Canonical Allele Identifier: CA2424676661
Gene: CYBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783923G= , CM000685.2:g.37783923G= GRCh38
NC_000023.10:g.37643176G= , CM000685.1:g.37643176G= GRCh37
NC_000023.9:g.37528120G= NCBI36
NG_009065.1:g.8907G= , LRG_53:g.8907G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+323G= ENSP00000512461.1:n.252+323G=
ENST00000696171.1:c.156+323G= ENSP00000512462.1:n.156+323G=
ENST00000696172.1:c.252+323G= ENSP00000512463.1:n.252+323G=
ENST00000696173.1:n.260+323G=
ENST00000378588.5:c.252+323G= MANE Select ENSP00000367851.4:n.252+323G=
ENST00000378588.4:c.252+323G= ENSP00000367851.4:n.252+323G=
ENST00000465127.1:c.171+357923G= ENSP00000417050.1:n.171+357923G=
NM_000397.3:c.252+323G= , LRG_53t1:c.252+323G= NP_000388.2:n.252+323G=
XM_011543890.1:c.-179+323G= XP_011542192.1:n.-179+323G=
NM_000397.4:c.252+323G= MANE Select NP_000388.2:n.252+323G=
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