Linked Data
dbSNP Id:
rs2080861904
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.36993314T>C , CM000665.2:g.36993314T>C | GRCh38 |
| NC_000003.11:g.37034805T>C , CM000665.1:g.37034805T>C | GRCh37 |
| NC_000003.10:g.37009809T>C | NCBI36 |
| NG_007109.2:g.4965T>C , LRG_216:g.4965T>C | |
| NG_008418.1:g.4991A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673673.2:c.-234T>C | ENSP00000500979.2:n.-234T>C |