Linked Data
dbSNP Id:
rs1798172625
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.11491410T>G , CM000670.2:g.11491410T>G | GRCh38 |
| NC_000008.10:g.11348919T>G , CM000670.1:g.11348919T>G | GRCh37 |
| NC_000008.9:g.11386328T>G | NCBI36 |
| NG_023543.1:g.2399T>G | |
| NG_023543.2:g.2399T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696154.2:n.274+4243T>G | ||
| ENST00000696154.1:c.-91+4243T>G | ENSP00000512445.1:n.-91+4243T>G | |
| ENST00000645242.1:c.-91+4243T>G | ENSP00000494690.1:n.-91+4243T>G |