Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152806050C= , CM000663.2:g.152806050C= | GRCh38 |
| NC_000001.10:g.152778526C= , CM000663.1:g.152778526C= | GRCh37 |
| NC_000001.9:g.151045150C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_178351.4:c.-20-552G= MANE Select | NP_848128.1:n.-20-552G= |
| ENST00000607093.2:c.-20-552G= MANE Select | ENSP00000475270.1:n.-20-552G= |
| NM_001276331.1:c.-20-552G= | NP_001263260.1:n.-20-552G= |
| NM_001276331.2:c.-20-552G= | NP_001263260.1:n.-20-552G= |
| NM_178351.3:c.-20-552G= | NP_848128.1:n.-20-552G= |
| ENST00000606576.1:c.-20-552G= | ENSP00000476034.1:n.-20-552G= |