Linked Data
ClinVar Variation Id:
200190
dbSNP Id:
rs773204216
ExAC:
15:48736750 C / T
gnomAD v2:
15-48736750-C-T
gnomAD v3:
15-48444553-C-T
gnomAD v4:
15-48444553-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48444553C>T , CM000677.2:g.48444553C>T | GRCh38 |
| NC_000015.9:g.48736750C>T , CM000677.1:g.48736750C>T | GRCh37 |
| NC_000015.8:g.46524042C>T | NCBI36 |
| NG_008805.2:g.206236G>A , LRG_778:g.206236G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.6025G>A | ENSP00000453958.2:p.Glu2009Lys | |
| ENST00000674301.2:c.6025G>A | ENSP00000501333.2:p.Glu2009Lys | |
| ENST00000684448.1:n.4699G>A | ||
| ENST00000316623.10:c.6025G>A MANE Select | ENSP00000325527.5:p.Glu2009Lys | |
| ENST00000674301.1:c.1024G>A | ENSP00000501333.1:p.Glu342Lys | |
| ENST00000316623.9:c.6025G>A | ENSP00000325527.5:p.Glu2009Lys | |
| ENST00000537463.6:c.*1788G>A | ENSP00000440294.2:n.*1788G>A | |
| ENST00000559133.5:c.1332G>A | ||
| ENST00000560820.1:n.145G>A | ||
| NM_000138.4:c.6025G>A , LRG_778t1:c.6025G>A | NP_000129.3:p.Glu2009Lys | |
| NM_000138.5:c.6025G>A MANE Select | NP_000129.3:p.Glu2009Lys |