Canonical Allele Identifier: CA412977005
Gene: CYBB HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37663129G>C (hg19) chrX:g.37803876G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37803876G>C , CM000685.2:g.37803876G>C GRCh38
NC_000023.10:g.37663129G>C , CM000685.1:g.37663129G>C GRCh37
NC_000023.9:g.37548073G>C NCBI36
NG_009065.1:g.28860G>C , LRG_53:g.28860G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*407-1G>C ENSP00000512461.1:n.*407-1G>C
ENST00000696171.1:c.802-1G>C ENSP00000512462.1:n.802-1G>C
ENST00000378588.5:c.898-1G>C MANE Select ENSP00000367851.4:n.898-1G>C
ENST00000378588.4:c.898-1G>C ENSP00000367851.4:n.898-1G>C
ENST00000465127.1:c.171+377876G>C ENSP00000417050.1:n.171+377876G>C
ENST00000492288.1:n.323-1G>C
NM_000397.3:c.898-1G>C , LRG_53t1:c.898-1G>C NP_000388.2:n.898-1G>C
XM_011543890.1:c.592-1G>C XP_011542192.1:n.592-1G>C
NM_000397.4:c.898-1G>C MANE Select NP_000388.2:n.898-1G>C
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