Linked Data
ClinVar Variation Id:
387211
dbSNP Id:
rs771093927
ExAC:
5:148406319 A / T
gnomAD v2:
5-148406319-A-T
gnomAD v3:
5-149026756-A-T
gnomAD v4:
5-149026756-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149026756A>T , CM000667.2:g.149026756A>T | GRCh38 |
| NC_000005.9:g.148406319A>T , CM000667.1:g.148406319A>T | GRCh37 |
| NC_000005.8:g.148386512A>T | NCBI36 |
| NG_007947.2:g.41419T>A , LRG_269:g.41419T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.2769-4T>A | ||
| ENST00000515425.6:c.2873-4T>A MANE Select | ENSP00000423660.1:n.2873-4T>A | |
| ENST00000675793.1:c.*2157-4T>A | ENSP00000502039.1:n.*2157-4T>A | |
| ENST00000676056.1:c.*2383-4T>A | ENSP00000501827.1:n.*2383-4T>A | |
| ENST00000323829.9:c.*2261-4T>A | ENSP00000313025.5:n.*2261-4T>A | |
| ENST00000504517.5:c.2403-4T>A | ENSP00000421779.1:n.2403-4T>A | |
| ENST00000504690.5:c.2873-4T>A | ENSP00000425627.1:n.2873-4T>A | |
| ENST00000510779.1:c.1923-4T>A | ||
| ENST00000511307.5:c.*2756T>A | ENSP00000421420.1:n.*2756T>A | |
| ENST00000512049.5:c.2852-4T>A | ENSP00000421860.1:n.2852-4T>A | |
| ENST00000513604.5:c.*2364T>A | ENSP00000423111.1:n.*2364T>A | |
| ENST00000515425.5:c.2873-4T>A | ENSP00000423660.1:n.2873-4T>A | |
| NM_024577.3:c.2873-4T>A , LRG_269t1:c.2873-4T>A | NP_078853.2:n.2873-4T>A | |
| NM_024577.4:c.2873-4T>A MANE Select | NP_078853.2:n.2873-4T>A |