Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612640A>T , CM000679.2:g.41612640A>T | GRCh38 |
| NC_000017.10:g.39768892A>T , CM000679.1:g.39768892A>T | GRCh37 |
| NC_000017.9:g.37022418A>T | NCBI36 |
| NG_008301.1:g.5188T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.49T>A MANE Select | ENSP00000301653.3:p.Ser17Thr | |
| ENST00000301653.8:c.49T>A | ENSP00000301653.3:p.Ser17Thr | |
| ENST00000588319.1:n.126T>A | ||
| ENST00000590990.1:c.49T>A | ENSP00000467105.1:p.Ser17Thr | |
| ENST00000593067.1:c.-313+150T>A | ENSP00000467124.1:n.-313+150T>A | |
| NM_005557.3:c.49T>A | NP_005548.2:p.Ser17Thr | |
| NM_005557.4:c.49T>A MANE Select | NP_005548.2:p.Ser17Thr |