Linked Data
dbSNP Id:
rs186514943
gnomAD v2:
9-130582417-A-G
gnomAD v3:
9-127820138-A-G
gnomAD v4:
9-127820138-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127820138A>G , CM000671.2:g.127820138A>G | GRCh38 |
| NC_000009.11:g.130582417A>G , CM000671.1:g.130582417A>G | GRCh37 |
| NC_000009.10:g.129622238A>G | NCBI36 |
| NG_009551.1:g.39631T>C , LRG_589:g.39631T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480266.6:c.589-101T>C | ENSP00000479015.1:n.589-101T>C | |
| ENST00000373203.9:c.1135-101T>C MANE Select | ENSP00000362299.4:n.1135-101T>C | |
| ENST00000344849.4:c.1135-101T>C | ENSP00000341917.3:n.1135-101T>C | |
| ENST00000373203.8:c.1135-101T>C | ENSP00000362299.4:n.1135-101T>C | |
| ENST00000480266.5:c.589-101T>C | ENSP00000479015.1:n.589-101T>C | |
| ENST00000486329.1:n.103-101T>C | ||
| NM_000118.3:c.1135-101T>C , LRG_589t1:c.1135-101T>C | NP_000109.1:n.1135-101T>C | |
| NM_001114753.2:c.1135-101T>C , LRG_589t2:c.1135-101T>C | NP_001108225.1:n.1135-101T>C | |
| NM_001278138.1:c.589-101T>C | NP_001265067.1:n.589-101T>C | |
| NR_136302.1:n.1569-1057A>G | ||
| NM_001114753.3:c.1135-101T>C MANE Select | NP_001108225.1:n.1135-101T>C | |
| NM_001278138.2:c.589-101T>C | NP_001265067.1:n.589-101T>C |