Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.40688678G>C , CM000682.2:g.40688678G>C | GRCh38 |
| NC_000020.10:g.39317318G>C , CM000682.1:g.39317318G>C | GRCh37 |
| NC_000020.9:g.38750732G>C | NCBI36 |
| NG_023378.1:g.5559C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005461.5:c.173C>G MANE Select | NP_005452.2:p.Thr58Arg |
| ENST00000373313.3:c.173C>G MANE Select | ENSP00000362410.2:p.Thr58Arg |
| NM_005461.4:c.173C>G | NP_005452.2:p.Thr58Arg |
| ENST00000373313.2:c.173C>G | ENSP00000362410.2:p.Thr58Arg |