dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.18992540G>A , CM000686.2:g.18992540G>A | GRCh38 |
| NC_000024.9:g.21154426G>A , CM000686.1:g.21154426G>A | GRCh37 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382840.3:n.170C>T (CD24P4) | ||
| NR_125733.1:n.579-59065C>T (TTTY14) | ||
| NR_125734.1:n.578+76184C>T (TTTY14) | ||
| NR_125735.1:n.503+84505C>T (TTTY14) | ||
| NR_125736.1:n.138+76184C>T (TTTY14) | ||
| NR_125737.1:n.139-59699C>T (TTTY14) | ||
| NR_001543.4:n.504-59699C>T (TTTY14) | ||
| NR_125737.2:n.139-59699C>T (TTTY14) | ||
| NR_158640.1:n.152+80959C>T (TTTY14) | ||
| NR_158641.1:n.368+52002C>T (TTTY14) |