Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45095436C>T , CM000677.2:g.45095436C>T | GRCh38 |
| NC_000015.9:g.45387634C>T , CM000677.1:g.45387634C>T | GRCh37 |
| NC_000015.8:g.43174926C>T | NCBI36 |
| NG_009447.1:g.23726G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001363711.2:c.4239+1G>A MANE Select | NP_001350640.1:n.4239+1G>A |
| ENST00000389039.11:c.4239+1G>A MANE Select | ENSP00000373691.7:n.4239+1G>A |
| NM_001363711.1:c.4239+1G>A | NP_001350640.1:n.4239+1G>A |
| NM_014080.4:c.4239+1G>A | NP_054799.4:n.4239+1G>A |
| NM_014080.5:c.4239+1G>A | NP_054799.4:n.4239+1G>A |
| ENST00000389039.10:c.4239+1G>A | ENSP00000373691.6:n.4239+1G>A |
| ENST00000603300.1:c.4239+1G>A | ENSP00000475084.1:n.4239+1G>A |
| XM_005254421.2:c.4239+1G>A | XP_005254478.1:n.4239+1G>A |