Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35842469C>T , CM000681.2:g.35842469C>T | GRCh38 |
| NC_000019.9:g.36333371C>T , CM000681.1:g.36333371C>T | GRCh37 |
| NC_000019.8:g.41025211C>T | NCBI36 |
| NG_013356.2:g.31819G>A , LRG_693:g.31819G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.2416G>A MANE Select | NP_004637.1:p.Ala806Thr |
| ENST00000378910.10:c.2416G>A MANE Select | ENSP00000368190.4:p.Ala806Thr |
| NM_004646.3:c.2416G>A , LRG_693t1:c.2416G>A | NP_004637.1:p.Ala806Thr |
| ENST00000353632.6:c.2416G>A | ENSP00000343634.5:p.Ala806Thr |
| ENST00000378910.9:c.2416G>A | ENSP00000368190.4:p.Ala806Thr |