Linked Data
dbSNP Id:
rs894063132
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17129703T>G , CM000672.2:g.17129703T>G | GRCh38 |
| NC_000010.10:g.17171702T>G , CM000672.1:g.17171702T>G | GRCh37 |
| NC_000010.9:g.17211708T>G | NCBI36 |
| NG_008967.1:g.5115A>C , LRG_540:g.5115A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.63A>C MANE Select | ENSP00000367064.4:p.Val21= | |
| ENST00000377823.1:c.63A>C | ENSP00000367054.1:p.Val21= | |
| ENST00000377833.8:c.63A>C | ENSP00000367064.4:p.Val21= | |
| NM_001081.3:c.63A>C , LRG_540t1:c.63A>C | NP_001072.2:p.Val21= | |
| XM_011519708.1:c.63A>C | XP_011518010.1:p.Val21= | |
| XM_011519708.2:c.63A>C | XP_011518010.1:p.Val21= | |
| NM_001081.4:c.63A>C MANE Select | NP_001072.2:p.Val21= |