Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35312404A>T , CM000668.2:g.35312404A>T | GRCh38 |
| NC_000006.11:g.35280181A>T , CM000668.1:g.35280181A>T | GRCh37 |
| NC_000006.10:g.35388159A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000444278.3:c.415A>T | ENSP00000415357.3:p.Thr139Ser | |
| ENST00000698929.1:c.423+1760A>T | ENSP00000514040.1:n.423+1760A>T | |
| ENST00000698930.1:c.*173A>T | ENSP00000514041.1:n.*173A>T | |
| ENST00000698931.1:n.550A>T | ||
| ENST00000316637.7:c.526A>T MANE Select | ENSP00000319831.5:p.Thr176Ser | |
| ENST00000316637.6:c.526A>T | ENSP00000319831.5:p.Thr176Ser | |
| ENST00000444278.2:c.251A>T | ||
| NM_022047.3:c.526A>T | NP_071330.3:p.Thr176Ser | |
| NM_022047.4:c.526A>T MANE Select | NP_071330.3:p.Thr176Ser |