Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119514622A>T , CM000663.2:g.119514622A>T | GRCh38 |
| NC_000001.10:g.120057245A>T , CM000663.1:g.120057245A>T | GRCh37 |
| NC_000001.9:g.119858768A>T | NCBI36 |
| NG_050909.1:g.12511A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000862.3:c.1099A>T MANE Select | NP_000853.1:p.Thr367Ser |
| ENST00000369413.8:c.1099A>T MANE Select | ENSP00000358421.3:p.Thr367Ser |
| NM_000862.2:c.1099A>T | NP_000853.1:p.Thr367Ser |
| NM_001328615.1:c.1099A>T | NP_001315544.1:p.Thr367Ser |
| ENST00000369413.7:c.1099A>T | ENSP00000358421.3:p.Thr367Ser |
| ENST00000528909.1:c.1099A>T | ENSP00000432268.1:p.Thr367Ser |
| XM_011541314.1:c.1105A>T | XP_011539616.1:p.Thr369Ser |