Linked Data
dbSNP Id:
rs1895887560
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56041911T>C , CM000674.2:g.56041911T>C | GRCh38 |
| NC_000012.11:g.56435695T>C , CM000674.1:g.56435695T>C | GRCh37 |
| NC_000012.10:g.54721962T>C | NCBI36 |
| NG_023201.1:g.5010T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-256T>C | ENSP00000348849.5:n.-256T>C | |
| ENST00000356464.9:c.-256T>C | ENSP00000348849.5:n.-256T>C | |
| ENST00000552361.1:c.-188T>C | ENSP00000450339.1:n.-188T>C | |
| NM_001029.3:c.-256T>C | NP_001020.2:n.-256T>C | |
| XR_944989.3:n.93A>G | ||
| XR_944990.3:n.93A>G |