Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075574C>T , CM000679.2:g.8075574C>T | GRCh38 |
| NC_000017.10:g.7978892C>T , CM000679.1:g.7978892C>T | GRCh37 |
| NC_000017.9:g.7919617C>T | NCBI36 |
| NG_007099.1:g.17130G>A | |
| NG_007099.2:g.17143G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1654+21G>A MANE Select | ENSP00000497784.1:n.1654+21G>A | |
| ENST00000649809.1:c.718+21G>A | ENSP00000496845.1:n.718+21G>A | |
| ENST00000319144.4:c.1654+21G>A | ENSP00000315167.4:n.1654+21G>A | |
| ENST00000577351.5:n.479+601G>A | ||
| NM_001139.2:c.1654+21G>A | NP_001130.1:n.1654+21G>A | |
| NM_001139.3:c.1654+21G>A MANE Select | NP_001130.1:n.1654+21G>A |