Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.44942060T= , CM000664.2:g.44942060T= | GRCh38 |
| NC_000002.11:g.45169199T= , CM000664.1:g.45169199T= | GRCh37 |
| NC_000002.10:g.45022703T= | NCBI36 |
| NG_016222.1:g.5163T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260653.5:c.-45T= MANE Select | ENSP00000260653.3:n.-45T= | |
| ENST00000260653.4:c.-45T= | ENSP00000260653.3:n.-45T= | |
| NM_005413.3:c.-45T= | NP_005404.1:n.-45T= | |
| XM_011533042.1:c.-45T= | XP_011531344.1:n.-45T= | |
| NM_005413.4:c.-45T= MANE Select | NP_005404.1:n.-45T= |