Canonical Allele Identifier: CA515675584
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37663285T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804032T>C , CM000685.2:g.37804032T>C GRCh38
NC_000023.10:g.37663285T>C , CM000685.1:g.37663285T>C GRCh37
NC_000023.9:g.37548229T>C NCBI36
NG_009065.1:g.29016T>C , LRG_53:g.29016T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*562T>C ENSP00000512461.1:n.*562T>C
ENST00000696171.1:c.957T>C ENSP00000512462.1:p.Phe319=
ENST00000378588.5:c.1053T>C MANE Select ENSP00000367851.4:p.Phe351=
ENST00000378588.4:c.1053T>C ENSP00000367851.4:p.Phe351=
ENST00000465127.1:c.171+378032T>C ENSP00000417050.1:n.171+378032T>C
ENST00000492288.1:n.478T>C
NM_000397.3:c.1053T>C , LRG_53t1:c.1053T>C NP_000388.2:p.Phe351=
XM_011543890.1:c.747T>C XP_011542192.1:p.Phe249=
NM_000397.4:c.1053T>C MANE Select NP_000388.2:p.Phe351=
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