Linked Data
dbSNP Id:
rs1861927512
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112025377G>A , CM000673.2:g.112025377G>A | GRCh38 |
| NC_000011.9:g.111896101G>A , CM000673.1:g.111896101G>A | GRCh37 |
| NC_000011.8:g.111401311G>A | NCBI36 |
| NG_013342.1:g.5564G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713569.1:c.-96G>A | ENSP00000518862.1:n.-96G>A | |
| ENST00000280346.10:c.-96G>A | ENSP00000280346.6:n.-96G>A | |
| NM_001931.4:c.-96G>A | NP_001922.2:n.-96G>A | |
| XM_011542647.1:c.-96G>A | XP_011540949.1:n.-96G>A |