Linked Data
dbSNP Id:
rs1848921431
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893485G>A , CM000673.2:g.14893485G>A | GRCh38 |
| NC_000011.9:g.14915031G>A , CM000673.1:g.14915031G>A | GRCh37 |
| NC_000011.8:g.14871607G>A | NCBI36 |
| NG_007936.1:g.3721C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.1:c.-1241C>T | XP_011518200.1:n.-1241C>T | |
| XM_011519898.3:c.-1241C>T | XP_011518200.1:n.-1241C>T |