Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.8811899T>C , CM000686.2:g.8811899T>C | GRCh38 |
| NC_000024.9:g.8679940T>C , CM000686.1:g.8679940T>C | GRCh37 |
| NC_000024.8:g.8739940T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253470.4:n.37+5447A>G | ||
| NR_001548.2:n.37+5447A>G |