Linked Data
dbSNP Id:
rs1587552089
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.83549033C>T , CM000671.2:g.83549033C>T | GRCh38 |
| NC_000009.11:g.86163948C>T , CM000671.1:g.86163948C>T | GRCh37 |
| NC_000009.10:g.85353768C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017014588.1:c.24+11137G>A | XP_016870077.1:n.24+11137G>A | |
| XM_024447487.1:c.-142+25877G>A | XP_024303255.1:n.-142+25877G>A | |
| XM_024447489.1:c.-142+25877G>A | XP_024303257.1:n.-142+25877G>A |