Linked Data
dbSNP Id:
rs1280659857
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536422G>C , CM000679.2:g.42536422G>C | GRCh38 |
| NC_000017.10:g.40688440G>C , CM000679.1:g.40688440G>C | GRCh37 |
| NC_000017.9:g.37941966G>C | NCBI36 |
| NG_011552.1:g.5490G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.150G>C MANE Select | ENSP00000225927.1:p.Val50= | |
| ENST00000225927.6:c.150G>C | ENSP00000225927.1:p.Val50= | |
| NM_000263.3:c.150G>C | NP_000254.2:p.Val50= | |
| XM_024450771.1:c.150G>C | XP_024306539.1:p.Val50= | |
| NM_000263.4:c.150G>C MANE Select | NP_000254.2:p.Val50= |