Linked Data
dbSNP Id:
rs117096873
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11293103C>G , CM000678.2:g.11293103C>G | GRCh38 |
| NC_000016.9:g.11386960C>G , CM000678.1:g.11386960C>G | GRCh37 |
| NC_000016.8:g.11294461C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+43325C>G | ||
| ENST00000572173.1:c.-515-2113C>G | ENSP00000461206.1:n.-515-2113C>G | |
| ENST00000573910.1:n.161-23349C>G | ||
| XR_933070.1:n.733+43325C>G | ||
| XR_933070.3:n.876+43325C>G |