Linked Data
dbSNP Id:
rs1836951847
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350550A>G , CM000672.2:g.47350550A>G | GRCh38 |
| NC_000010.10:g.48388812T>C , CM000672.1:g.48388812T>C | GRCh37 |
| NC_000010.9:g.48008818T>C | NCBI36 |
| NG_029718.1:g.7180A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.2066A>G MANE Select | ENSP00000463151.1:p.Asp689Gly | |
| ENST00000584701.1:c.2066A>G | ENSP00000463151.1:p.Asp689Gly | |
| NM_002900.2:c.2066A>G | NP_002891.1:p.Asp689Gly | |
| NM_002900.3:c.2066A>G MANE Select | NP_002891.1:p.Asp689Gly |