Linked Data
dbSNP Id:
rs2241820
gnomAD v2:
12-54394497-C-A
gnomAD v3:
12-54000713-C-A
gnomAD v4:
12-54000713-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.54000713C>A , CM000674.2:g.54000713C>A | GRCh38 |
| NC_000012.11:g.54394497C>A , CM000674.1:g.54394497C>A | GRCh37 |
| NC_000012.10:g.52680764C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303450.5:c.525C>A (HOXC9) MANE Select | ENSP00000302836.4:p.Ala175= | |
| ENST00000303450.4:c.525C>A (HOXC9) | ENSP00000302836.4:p.Ala175= | |
| ENST00000504315.1:c.-193+9899C>A (HOXC6) | ENSP00000424124.1:n.-193+9899C>A | |
| ENST00000504557.1:n.123-1717C>A (HOXC9) | ||
| ENST00000508190.1:c.525C>A (HOXC9) | ENSP00000423861.1:p.Ala175= | |
| ENST00000509328.1:c.-73+5697C>A (HOXC6) | ENSP00000423898.1:n.-73+5697C>A | |
| ENST00000513209.1:c.166+14703C>A | ENSP00000476742.1:n.166+14703C>A | |
| NM_006897.1:c.525C>A (HOXC9) | NP_008828.1:p.Ala175= | |
| NM_006897.2:c.525C>A (HOXC9) | NP_008828.1:p.Ala175= | |
| NM_006897.3:c.525C>A (HOXC9) MANE Select | NP_008828.1:p.Ala175= |