Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749069T= , CM000677.2:g.74749069T= | GRCh38 |
| NC_000015.9:g.75041410T= , CM000677.1:g.75041410T= | GRCh37 |
| NC_000015.8:g.72828463T= | NCBI36 |
| NG_008431.1:g.31528T= | |
| NG_008431.2:g.31528T= | |
| NG_061543.1:g.5225T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.-10+172T= MANE Select | ENSP00000342007.4:n.-10+172T= | |
| ENST00000343932.4:c.-10+172T= | ENSP00000342007.4:n.-10+172T= | |
| NM_000761.4:c.-10+172T= | NP_000752.2:n.-10+172T= | |
| NM_000761.5:c.-10+172T= MANE Select | NP_000752.2:n.-10+172T= |