Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.47572783T= , CM000685.2:g.47572783T= | GRCh38 |
| NC_000023.10:g.47432182T= , CM000685.1:g.47432182T= | GRCh37 |
| NC_000023.9:g.47317126T= | NCBI36 |
| NG_008437.1:g.52075A= | |
| NG_016339.1:g.16667T= | |
| NG_016339.2:g.16667T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295987.13:c.*81A= MANE Select | ENSP00000295987.7:n.*81A= | |
| ENST00000340666.5:c.*151A= | ENSP00000343206.4:n.*151A= | |
| ENST00000640721.1:c.249A= | ENSP00000492857.1:n.249A= | |
| ENST00000295987.11:c.*81A= | ENSP00000295987.7:n.*81A= | |
| ENST00000340666.4:c.*151A= | ENSP00000343206.4:n.*151A= | |
| NM_006950.3:c.*81A= MANE Select | NP_008881.2:n.*81A= | |
| NM_133499.2:c.*151A= | NP_598006.1:n.*151A= |