Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144342G>A , CM000670.2:g.38144342G>A | GRCh38 |
| NC_000008.10:g.38001860G>A , CM000670.1:g.38001860G>A | GRCh37 |
| NC_000008.9:g.38121017G>A | NCBI36 |
| NG_011827.1:g.11741C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.789C>T MANE Select | ENSP00000276449.3:p.Thr263= | |
| ENST00000276449.8:c.789C>T | ENSP00000276449.3:p.Thr263= | |
| ENST00000520114.1:n.2758C>T | ||
| ENST00000522050.1:c.631C>T | ||
| NM_000349.2:c.789C>T | NP_000340.2:p.Thr263= | |
| XM_006716392.1:c.695C>T | XP_006716455.1:p.Pro232Leu | |
| NM_000349.3:c.789C>T MANE Select | NP_000340.2:p.Thr263= |