Linked Data
dbSNP Id:
rs876660222
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403034G>C , CM000664.2:g.47403034G>C | GRCh38 |
| NC_000002.11:g.47630173G>C , CM000664.1:g.47630173G>C | GRCh37 |
| NC_000002.10:g.47483677G>C | NCBI36 |
| NG_007110.2:g.4911G>C , LRG_218:g.4911G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233146.6:c.-158G>C | ENSP00000233146.2:n.-158G>C |