Linked Data
dbSNP Id:
rs1572377325
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31583831A>C , CM000664.2:g.31583831A>C | GRCh38 |
| NC_000002.11:g.31808900A>C , CM000664.1:g.31808900A>C | GRCh37 |
| NC_000002.10:g.31662404A>C | NCBI36 |
| NG_008365.1:g.2141T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011533070.1:c.27-50065T>G | XP_011531372.1:n.27-50065T>G | |
| XM_011533071.1:c.27-50065T>G | XP_011531373.1:n.27-50065T>G | |
| XM_011533072.1:c.27-50065T>G | XP_011531374.1:n.27-50065T>G | |
| XM_011533072.2:c.27-50065T>G | XP_011531374.1:n.27-50065T>G |