Linked Data
ClinVar Variation Id:
1705199
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.92719028G>C , CM000671.2:g.92719028G>C | GRCh38 |
| NC_000009.11:g.95481310G>C , CM000671.1:g.95481310G>C | GRCh37 |
| NC_000009.10:g.94521131G>C | NCBI36 |
| NG_033908.1:g.50774C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356884.11:c.1617C>G MANE Select | ENSP00000349351.6:p.His539Gln | |
| ENST00000356884.10:c.1617C>G | ENSP00000349351.6:p.His539Gln | |
| ENST00000375512.3:c.1617C>G | ENSP00000364662.3:p.His539Gln | |
| NM_001003800.1:c.1617C>G | NP_001003800.1:p.His539Gln | |
| NM_015250.3:c.1617C>G | NP_056065.1:p.His539Gln | |
| XM_017014551.1:c.1698C>G | XP_016870040.1:p.His566Gln | |
| NM_001003800.2:c.1617C>G MANE Select | NP_001003800.1:p.His539Gln | |
| NM_015250.4:c.1617C>G | NP_056065.1:p.His539Gln |