Linked Data
dbSNP Id:
rs1756866058
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.147854946T>C , CM000667.2:g.147854946T>C | GRCh38 |
| NC_000005.9:g.147234509T>C , CM000667.1:g.147234509T>C | GRCh37 |
| NC_000005.8:g.147214702T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017009459.1:c.261-4404A>G | XP_016864948.1:n.261-4404A>G |