Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.92718570G>C , CM000671.2:g.92718570G>C | GRCh38 |
| NC_000009.11:g.95480852G>C , CM000671.1:g.95480852G>C | GRCh37 |
| NC_000009.10:g.94520673G>C | NCBI36 |
| NG_033908.1:g.51232C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356884.11:c.2075C>G MANE Select | ENSP00000349351.6:p.Thr692Arg | |
| ENST00000356884.10:c.2075C>G | ENSP00000349351.6:p.Thr692Arg | |
| ENST00000375512.3:c.2075C>G | ENSP00000364662.3:p.Thr692Arg | |
| NM_001003800.1:c.2075C>G | NP_001003800.1:p.Thr692Arg | |
| NM_015250.3:c.2075C>G | NP_056065.1:p.Thr692Arg | |
| XM_017014551.1:c.2156C>G | XP_016870040.1:p.Thr719Arg | |
| NM_001003800.2:c.2075C>G MANE Select | NP_001003800.1:p.Thr692Arg | |
| NM_015250.4:c.2075C>G | NP_056065.1:p.Thr692Arg |