COSMIC:
COSM3749220 (not active)
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.72563473 (EAS)
Genomes Max Group AF
0.74300332 (EAS)
Exomes Max Group AF
0.72085071 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.54000713C>T , CM000674.2:g.54000713C>T | GRCh38 |
| NC_000012.11:g.54394497C>T , CM000674.1:g.54394497C>T | GRCh37 |
| NC_000012.10:g.52680764C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303450.5:c.525C>T (HOXC9) MANE Select | ENSP00000302836.4:p.Ala175= | |
| ENST00000303450.4:c.525C>T (HOXC9) | ENSP00000302836.4:p.Ala175= | |
| ENST00000504315.1:c.-193+9899C>T (HOXC6) | ENSP00000424124.1:n.-193+9899C>T | |
| ENST00000504557.1:n.123-1717C>T (HOXC9) | ||
| ENST00000508190.1:c.525C>T (HOXC9) | ENSP00000423861.1:p.Ala175= | |
| ENST00000509328.1:c.-73+5697C>T (HOXC6) | ENSP00000423898.1:n.-73+5697C>T | |
| ENST00000513209.1:c.166+14703C>T | ENSP00000476742.1:n.166+14703C>T | |
| NM_006897.1:c.525C>T (HOXC9) | NP_008828.1:p.Ala175= | |
| NM_006897.2:c.525C>T (HOXC9) | NP_008828.1:p.Ala175= | |
| NM_006897.3:c.525C>T (HOXC9) MANE Select | NP_008828.1:p.Ala175= |