Linked Data
dbSNP Id:
rs2103111129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193122025T>C , CM000663.2:g.193122025T>C | GRCh38 |
| NC_000001.10:g.193091155T>C , CM000663.1:g.193091155T>C | GRCh37 |
| NC_000001.9:g.191357778T>C | NCBI36 |
| NG_012691.1:g.5068T>C , LRG_507:g.5068T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643006.1:c.-176T>C | ENSP00000496633.1:n.-176T>C | |
| ENST00000649895.1:n.43T>C | ||
| ENST00000367435.3:c.-176T>C | ENSP00000356405.3:n.-176T>C | |
| NM_024529.4:c.-176T>C , LRG_507t1:c.-176T>C | NP_078805.3:n.-176T>C | |
| XR_001738350.1:n.1632A>G |