Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6145623A>G , CM000668.2:g.6145623A>G | GRCh38 |
| NC_000006.11:g.6145856A>G , CM000668.1:g.6145856A>G | GRCh37 |
| NC_000006.10:g.6090855A>G | NCBI36 |
| NG_008107.1:g.180069T>C , LRG_549:g.180069T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.2195T>C MANE Select | ENSP00000264870.3:p.Met732Thr | |
| ENST00000264870.7:c.2195T>C | ENSP00000264870.3:p.Met732Thr | |
| NM_000129.3:c.2195T>C , LRG_549t1:c.2195T>C | NP_000120.2:p.Met732Thr | |
| XM_006715010.2:c.2195T>C | XP_006715073.1:p.Met732Thr | |
| XM_011514342.1:c.2357T>C | XP_011512644.1:p.Met786Thr | |
| NM_000129.4:c.2195T>C MANE Select | NP_000120.2:p.Met732Thr |