Linked Data
dbSNP Id:
rs1422289570
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.3060671G>C , CM000666.2:g.3060671G>C | GRCh38 |
| NC_000004.11:g.3062398G>C , CM000666.1:g.3062398G>C | GRCh37 |
| NC_000004.10:g.3032196G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647962.1:n.825-1805G>C | ||
| ENST00000649900.1:n.503+18426G>C | ||
| ENST00000680239.1:c.5+18426G>C | ENSP00000506169.1:n.5+18426G>C | |
| ENST00000680360.1:c.5+18426G>C | ENSP00000505014.1:n.5+18426G>C | |
| ENST00000680956.1:c.5+18426G>C | ENSP00000506029.1:n.5+18426G>C | |
| ENST00000681528.1:c.5+18426G>C | ENSP00000506116.1:n.5+18426G>C |