Linked Data
ClinVar Variation Id:
237015
dbSNP Id:
rs201359896
ExAC:
9:130582323 C / T
gnomAD v2:
9-130582323-C-T
gnomAD v3:
9-127820044-C-T
gnomAD v4:
9-127820044-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127820044C>T , CM000671.2:g.127820044C>T | GRCh38 |
| NC_000009.11:g.130582323C>T , CM000671.1:g.130582323C>T | GRCh37 |
| NC_000009.10:g.129622144C>T | NCBI36 |
| NG_009551.1:g.39725G>A , LRG_589:g.39725G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000480266.6:c.589-7G>A | ENSP00000479015.1:n.589-7G>A | |
| ENST00000373203.9:c.1135-7G>A MANE Select | ENSP00000362299.4:n.1135-7G>A | |
| ENST00000344849.4:c.1135-7G>A | ENSP00000341917.3:n.1135-7G>A | |
| ENST00000373203.8:c.1135-7G>A | ENSP00000362299.4:n.1135-7G>A | |
| ENST00000480266.5:c.589-7G>A | ENSP00000479015.1:n.589-7G>A | |
| ENST00000486329.1:n.103-7G>A | ||
| NM_000118.3:c.1135-7G>A , LRG_589t1:c.1135-7G>A | NP_000109.1:n.1135-7G>A | |
| NM_001114753.2:c.1135-7G>A , LRG_589t2:c.1135-7G>A | NP_001108225.1:n.1135-7G>A | |
| NM_001278138.1:c.589-7G>A | NP_001265067.1:n.589-7G>A | |
| NR_136302.1:n.1569-1151C>T | ||
| NM_001114753.3:c.1135-7G>A MANE Select | NP_001108225.1:n.1135-7G>A | |
| NM_001278138.2:c.589-7G>A | NP_001265067.1:n.589-7G>A |