Linked Data
dbSNP Id:
rs557606920
ExAC:
15:80884056 C / T
gnomAD v2:
15-80884056-C-T
gnomAD v3:
15-80591715-C-T
gnomAD v4:
15-80591715-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80591715C>T , CM000677.2:g.80591715C>T | GRCh38 |
| NC_000015.9:g.80884056C>T , CM000677.1:g.80884056C>T | GRCh37 |
| NC_000015.8:g.78671111C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303329.9:c.2055+11C>T MANE Select | ENSP00000307479.4:n.2055+11C>T | |
| ENST00000303329.8:c.2055+11C>T | ENSP00000307479.4:n.2055+11C>T | |
| ENST00000527771.5:c.2022+11C>T | ENSP00000453792.1:n.2022+11C>T | |
| ENST00000533983.5:c.2022+11C>T | ENSP00000453651.1:n.2022+11C>T | |
| ENST00000610490.4:c.*353+11C>T | ENSP00000483762.1:n.*353+11C>T | |
| ENST00000622346.4:c.2055+11C>T | ENSP00000479393.1:n.2055+11C>T | |
| NM_014862.3:c.2055+11C>T | NP_055677.3:n.2055+11C>T | |
| NM_014862.4:c.2055+11C>T MANE Select | NP_055677.3:n.2055+11C>T |