Linked Data
dbSNP Id:
rs1688530652
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189004051A>T , CM000664.2:g.189004051A>T | GRCh38 |
| NC_000002.11:g.189868777A>T , CM000664.1:g.189868777A>T | GRCh37 |
| NC_000002.10:g.189577022A>T | NCBI36 |
| NG_007404.1:g.34679A>T , LRG_3:g.34679A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.2632A>T | ENSP00000415346.2:p.Thr878Ser | |
| ENST00000304636.9:c.2731A>T MANE Select | ENSP00000304408.4:p.Thr911Ser | |
| ENST00000304636.7:c.2731A>T | ENSP00000304408.3:p.Thr911Ser | |
| ENST00000317840.9:c.2527+1015A>T | ENSP00000315243.6:n.2527+1015A>T | |
| NM_000090.3:c.2731A>T , LRG_3t1:c.2731A>T | NP_000081.1:p.Thr911Ser | |
| NM_000090.4:c.2731A>T MANE Select | NP_000081.2:p.Thr911Ser |