Linked Data
dbSNP Id:
rs1785399178
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.37906548A>C , CM000669.2:g.37906548A>C | GRCh38 |
| NC_000007.13:g.37946150A>C , CM000669.1:g.37946150A>C | GRCh37 |
| NC_000007.12:g.37912675A>C | NCBI36 |
| NG_052980.1:g.15376T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436072.7:c.*931T>G (SFRP4) MANE Select | ENSP00000410715.2:n.*931T>G | |
| ENST00000436072.6:c.*931T>G (SFRP4) | ENSP00000410715.2:n.*931T>G | |
| ENST00000476620.1:c.-37-42292A>C (EPDR1) | ENSP00000425858.1:n.-37-42292A>C | |
| NM_003014.3:c.*931T>G (SFRP4) | NP_003005.2:n.*931T>G | |
| NM_003014.4:c.*931T>G (SFRP4) MANE Select | NP_003005.2:n.*931T>G |