Linked Data
dbSNP Id:
rs2120768003
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.63152009T>C , CM000674.2:g.63152009T>C | GRCh38 |
| NC_000012.11:g.63545789T>C , CM000674.1:g.63545789T>C | GRCh37 |
| NC_000012.10:g.61832056T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_000706.4:c.-1173A>G | NP_000697.1:n.-1173A>G | |
| XM_005269002.3:c.-1164A>G | XP_005269059.1:n.-1164A>G |