Linked Data
dbSNP Id:
rs2148571536
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3084169A>G , CM000682.2:g.3084169A>G | GRCh38 |
| NC_000020.10:g.3064815A>G , CM000682.1:g.3064815A>G | GRCh37 |
| NC_000020.9:g.3012815A>G | NCBI36 |
| NG_008663.1:g.5556T>C , LRG_715:g.5556T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.120+386T>C MANE Select | ENSP00000369647.3:n.120+386T>C | |
| NM_000490.4:c.120+386T>C , LRG_715t1:c.120+386T>C | NP_000481.2:n.120+386T>C | |
| XM_011529267.1:c.120+386T>C | XP_011527569.1:n.120+386T>C | |
| XM_011529267.2:c.120+386T>C | XP_011527569.1:n.120+386T>C | |
| NM_000490.5:c.120+386T>C MANE Select | NP_000481.2:n.120+386T>C |