Canonical Allele Identifier: CA412977291
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37663252T>G (hg19) chrX:g.37803999T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803999T>G , CM000685.2:g.37803999T>G GRCh38
NC_000023.10:g.37663252T>G , CM000685.1:g.37663252T>G GRCh37
NC_000023.9:g.37548196T>G NCBI36
NG_009065.1:g.28983T>G , LRG_53:g.28983T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*529T>G ENSP00000512461.1:n.*529T>G
ENST00000696171.1:c.924T>G ENSP00000512462.1:p.Phe308Leu
ENST00000378588.5:c.1020T>G MANE Select ENSP00000367851.4:p.Phe340Leu
ENST00000378588.4:c.1020T>G ENSP00000367851.4:p.Phe340Leu
ENST00000465127.1:c.171+377999T>G ENSP00000417050.1:n.171+377999T>G
ENST00000492288.1:n.445T>G
NM_000397.3:c.1020T>G , LRG_53t1:c.1020T>G NP_000388.2:p.Phe340Leu
XM_011543890.1:c.714T>G XP_011542192.1:p.Phe238Leu
NM_000397.4:c.1020T>G MANE Select NP_000388.2:p.Phe340Leu
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