Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96143340T= , CM000664.2:g.96143340T= | GRCh38 |
| NC_000002.11:g.96809079T= , CM000664.1:g.96809079T= | GRCh37 |
| NC_000002.10:g.96172806T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288943.5:c.*483A= MANE Select | ENSP00000288943.4:n.*483A= | |
| ENST00000288943.4:c.*483A= | ENSP00000288943.4:n.*483A= | |
| NM_004418.3:c.*483A= | NP_004409.1:n.*483A= | |
| XM_017003546.1:c.*483A= | XP_016859035.1:n.*483A= | |
| NM_004418.4:c.*483A= MANE Select | NP_004409.1:n.*483A= |