Linked Data
dbSNP Id:
rs72658197
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94423111G>T , CM000669.2:g.94423111G>T | GRCh38 |
| NC_000007.13:g.94052423G>T , CM000669.1:g.94052423G>T | GRCh37 |
| NC_000007.12:g.93890359G>T | NCBI36 |
| NG_007405.1:g.33551G>T , LRG_2:g.33551G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2558G>T MANE Select | ENSP00000297268.6:p.Gly853Val | |
| ENST00000297268.10:c.2558G>T | ENSP00000297268.6:p.Gly853Val | |
| ENST00000481570.5:n.641G>T | ||
| ENST00000497316.5:n.955G>T | ||
| ENST00000620463.1:c.2552G>T | ENSP00000477719.1:p.Gly851Val | |
| NM_000089.3:c.2558G>T , LRG_2t1:c.2558G>T | NP_000080.2:p.Gly853Val | |
| NM_000089.4:c.2558G>T MANE Select | NP_000080.2:p.Gly853Val |