Linked Data
dbSNP Id:
rs780814647
ExAC:
9:130586748 C / T
gnomAD v2:
9-130586748-C-T
gnomAD v4:
9-127824469-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127824469C>T , CM000671.2:g.127824469C>T | GRCh38 |
| NC_000009.11:g.130586748C>T , CM000671.1:g.130586748C>T | GRCh37 |
| NC_000009.10:g.129626569C>T | NCBI36 |
| NG_009551.1:g.35300G>A , LRG_589:g.35300G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480266.6:c.446-23G>A | ENSP00000479015.1:n.446-23G>A | |
| ENST00000373203.9:c.992-23G>A MANE Select | ENSP00000362299.4:n.992-23G>A | |
| ENST00000344849.4:c.992-23G>A | ENSP00000341917.3:n.992-23G>A | |
| ENST00000373203.8:c.992-23G>A | ENSP00000362299.4:n.992-23G>A | |
| ENST00000480266.5:c.446-23G>A | ENSP00000479015.1:n.446-23G>A | |
| NM_000118.3:c.992-23G>A , LRG_589t1:c.992-23G>A | NP_000109.1:n.992-23G>A | |
| NM_001114753.2:c.992-23G>A , LRG_589t2:c.992-23G>A | NP_001108225.1:n.992-23G>A | |
| NM_001278138.1:c.446-23G>A | NP_001265067.1:n.446-23G>A | |
| NM_001114753.3:c.992-23G>A MANE Select | NP_001108225.1:n.992-23G>A | |
| NM_001278138.2:c.446-23G>A | NP_001265067.1:n.446-23G>A |