Linked Data
dbSNP Id:
rs2144967736
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39243490C>T , CM000681.2:g.39243490C>T | GRCh38 |
| NC_000019.9:g.39734130C>T , CM000681.1:g.39734130C>T | GRCh37 |
| NC_000019.8:g.44425970C>T | NCBI36 |
| NG_042193.1:g.6482G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613087.5:c.*142G>A | ENSP00000481633.1:n.*142G>A | |
| NM_001346937.2:c.*142G>A | NP_001333866.1:n.*142G>A |