Linked Data
dbSNP Id:
rs13107806
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6269344T>A , CM000666.2:g.6269344T>A | GRCh38 |
| NC_000004.11:g.6271071T>A , CM000666.1:g.6271071T>A | GRCh37 |
| NC_000004.10:g.6321972T>A | NCBI36 |
| NG_011700.1:g.4495T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_017008586.1:c.4+7705T>A | XP_016864075.1:n.4+7705T>A |