Linked Data
ClinVar Variation Id:
1583106
ClinVar RCV Id:
RCV002097671
dbSNP Id:
rs368202311
gnomAD v2:
9-130581812-G-A
gnomAD v3:
9-127819533-G-A
gnomAD v4:
9-127819533-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127819533G>A , CM000671.2:g.127819533G>A | GRCh38 |
| NC_000009.11:g.130581812G>A , CM000671.1:g.130581812G>A | GRCh37 |
| NC_000009.10:g.129621633G>A | NCBI36 |
| NG_009551.1:g.40236C>T , LRG_589:g.40236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480266.6:c.765+89C>T | ENSP00000479015.1:n.765+89C>T | |
| ENST00000373203.9:c.1311+89C>T MANE Select | ENSP00000362299.4:n.1311+89C>T | |
| ENST00000344849.4:c.1311+89C>T | ENSP00000341917.3:n.1311+89C>T | |
| ENST00000373203.8:c.1311+89C>T | ENSP00000362299.4:n.1311+89C>T | |
| ENST00000480266.5:c.765+89C>T | ENSP00000479015.1:n.765+89C>T | |
| ENST00000486329.1:n.368C>T | ||
| NM_000118.3:c.1311+89C>T , LRG_589t1:c.1311+89C>T | NP_000109.1:n.1311+89C>T | |
| NM_001114753.2:c.1311+89C>T , LRG_589t2:c.1311+89C>T | NP_001108225.1:n.1311+89C>T | |
| NM_001278138.1:c.765+89C>T | NP_001265067.1:n.765+89C>T | |
| NR_136302.1:n.1568+822G>A | ||
| NM_001114753.3:c.1311+89C>T MANE Select | NP_001108225.1:n.1311+89C>T | |
| NM_001278138.2:c.765+89C>T | NP_001265067.1:n.765+89C>T |