Linked Data
dbSNP Id:
rs2134085810
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837523T>G , CM000672.2:g.102837523T>G | GRCh38 |
| NC_000010.10:g.104597280T>G , CM000672.1:g.104597280T>G | GRCh37 |
| NC_000010.9:g.104587270T>G | NCBI36 |
| NG_007955.1:g.5011A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.3:c.-162A>C | ENSP00000358903.3:n.-162A>C | |
| NM_000102.3:c.-162A>C | NP_000093.1:n.-162A>C |