Canonical Allele Identifier: CA2424676658
Gene: CYBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783917G= , CM000685.2:g.37783917G= GRCh38
NC_000023.10:g.37643170G= , CM000685.1:g.37643170G= GRCh37
NC_000023.9:g.37528114G= NCBI36
NG_009065.1:g.8901G= , LRG_53:g.8901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+317G= ENSP00000512461.1:n.252+317G=
ENST00000696171.1:c.156+317G= ENSP00000512462.1:n.156+317G=
ENST00000696172.1:c.252+317G= ENSP00000512463.1:n.252+317G=
ENST00000696173.1:n.260+317G=
ENST00000378588.5:c.252+317G= MANE Select ENSP00000367851.4:n.252+317G=
ENST00000378588.4:c.252+317G= ENSP00000367851.4:n.252+317G=
ENST00000465127.1:c.171+357917G= ENSP00000417050.1:n.171+357917G=
NM_000397.3:c.252+317G= , LRG_53t1:c.252+317G= NP_000388.2:n.252+317G=
XM_011543890.1:c.-179+317G= XP_011542192.1:n.-179+317G=
NM_000397.4:c.252+317G= MANE Select NP_000388.2:n.252+317G=
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