Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586479A>G , CM000679.2:g.41586479A>G | GRCh38 |
| NC_000017.10:g.39742731A>G , CM000679.1:g.39742731A>G | GRCh37 |
| NC_000017.9:g.36996257A>G | NCBI36 |
| NG_008624.1:g.5417T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000526.5:c.356T>C MANE Select | NP_000517.3:p.Met119Thr |
| ENST00000167586.7:c.356T>C MANE Select | ENSP00000167586.6:p.Met119Thr |
| NM_000526.4:c.356T>C | NP_000517.2:p.Met119Thr |
| ENST00000167586.6:c.356T>C | ENSP00000167586.6:p.Met119Thr |