Linked Data
dbSNP Id:
rs1809936771
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992503T>C , CM000670.2:g.16992503T>C | GRCh38 |
| NC_000008.10:g.16850012T>C , CM000670.1:g.16850012T>C | GRCh37 |
| NC_000008.9:g.16894383T>C | NCBI36 |
| NG_015978.1:g.14663A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*569A>G MANE Select | ENSP00000180166.5:n.*569A>G | |
| ENST00000180166.5:c.*569A>G | ENSP00000180166.5:n.*569A>G | |
| NM_019851.3:c.*569A>G MANE Select | NP_062825.1:n.*569A>G |