Linked Data
dbSNP Id:
rs1798172276
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.11491394G>A , CM000670.2:g.11491394G>A | GRCh38 |
| NC_000008.10:g.11348903G>A , CM000670.1:g.11348903G>A | GRCh37 |
| NC_000008.9:g.11386312G>A | NCBI36 |
| NG_023543.1:g.2383G>A | |
| NG_023543.2:g.2383G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696154.2:n.274+4227G>A | ||
| ENST00000696154.1:c.-91+4227G>A | ENSP00000512445.1:n.-91+4227G>A | |
| ENST00000645242.1:c.-91+4227G>A | ENSP00000494690.1:n.-91+4227G>A |