Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.52835481T= , CM000667.2:g.52835481T= | GRCh38 |
| NC_000005.9:g.52131315T= , CM000667.1:g.52131315T= | GRCh37 |
| NC_000005.8:g.52167072T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282588.7:c.62-13884T= MANE Select | ENSP00000282588.5:n.62-13884T= | |
| ENST00000650673.1:c.62-13884T= | ENSP00000498529.1:n.62-13884T= | |
| ENST00000282588.6:c.62-13884T= | ENSP00000282588.5:n.62-13884T= | |
| NM_181501.1:c.62-13884T= | NP_852478.1:n.62-13884T= | |
| NM_181501.2:c.62-13884T= MANE Select | NP_852478.1:n.62-13884T= |