Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837725T= , CM000685.2:g.154837725T= | GRCh38 |
| NC_000023.10:g.154066000T= , CM000685.1:g.154066000T= | GRCh37 |
| NC_000023.9:g.153719194T= | NCBI36 |
| NG_011403.1:g.189999A= | |
| NG_033065.1:g.1938A= | |
| NG_011403.2:g.189999A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6928A= MANE Select | ENSP00000353393.4:p.Thr2310= | |
| ENST00000644698.1:c.661A= | ENSP00000495706.1:p.Thr221= | |
| ENST00000330287.10:c.523A= | ENSP00000327895.6:p.Thr175= | |
| ENST00000360256.8:c.6928A= | ENSP00000353393.4:p.Thr2310= | |
| NM_000132.3:c.6928A= | NP_000123.1:p.Thr2310= | |
| NM_019863.2:c.523A= | NP_063916.1:p.Thr175= | |
| XM_011531126.1:c.6823A= | XP_011529428.1:p.Thr2275= | |
| NM_000132.4:c.6928A= MANE Select | NP_000123.1:p.Thr2310= | |
| NM_019863.3:c.523A= | NP_063916.1:p.Thr175= |