Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199436C>T , CM000671.2:g.137199436C>T | GRCh38 |
| NC_000009.11:g.140093888C>T , CM000671.1:g.140093888C>T | GRCh37 |
| NC_000009.10:g.139213709C>T | NCBI36 |
| NG_027801.1:g.6276G>A | |
| NG_027801.2:g.9758G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1276G>A MANE Select | ENSP00000387100.4:p.Ala426Thr | |
| ENST00000333046.8:c.670G>A | ENSP00000327617.4:p.Ala224Thr | |
| ENST00000409012.4:c.1276G>A | ENSP00000387100.4:p.Ala426Thr | |
| ENST00000541945.1:n.90+4668G>A | ||
| NM_001128228.2:c.1276G>A | NP_001121700.2:p.Ala426Thr | |
| NM_001128228.3:c.1276G>A MANE Select | NP_001121700.2:p.Ala426Thr |