Canonical Allele Identifier: CA412972836
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37642812G>A (hg19) chrX:g.37783559G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783559G>A , CM000685.2:g.37783559G>A GRCh38
NC_000023.10:g.37642812G>A , CM000685.1:g.37642812G>A GRCh37
NC_000023.9:g.37527756G>A NCBI36
NG_009065.1:g.8543G>A , LRG_53:g.8543G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.211G>A ENSP00000512461.1:p.Val71Ile
ENST00000696171.1:c.115G>A ENSP00000512462.1:p.Val39Ile
ENST00000696172.1:c.211G>A ENSP00000512463.1:p.Val71Ile
ENST00000696173.1:n.219G>A
ENST00000378588.5:c.211G>A MANE Select ENSP00000367851.4:p.Val71Ile
ENST00000378588.4:c.211G>A ENSP00000367851.4:p.Val71Ile
ENST00000465127.1:c.171+357559G>A ENSP00000417050.1:n.171+357559G>A
NM_000397.3:c.211G>A , LRG_53t1:c.211G>A NP_000388.2:p.Val71Ile
XM_011543890.1:c.-220G>A XP_011542192.1:n.-220G>A
NM_000397.4:c.211G>A MANE Select NP_000388.2:p.Val71Ile
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