Linked Data
ClinVar Variation Id:
318271
dbSNP Id:
rs9282732
ExAC:
16:1842386 C / T
gnomAD v2:
16-1842386-C-T
gnomAD v3:
16-1792385-C-T
gnomAD v4:
16-1792385-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1792385C>T , CM000678.2:g.1792385C>T | GRCh38 |
| NC_000016.9:g.1842386C>T , CM000678.1:g.1842386C>T | GRCh37 |
| NC_000016.8:g.1782387C>T | NCBI36 |
| NG_011778.1:g.6349G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215539.4:c.33G>A (IGFALS) MANE Select | ENSP00000215539.3:p.Ala11= | |
| ENST00000215539.3:c.33G>A (IGFALS) | ENSP00000215539.3:p.Ala11= | |
| ENST00000415638.3:c.147G>A (IGFALS) | ENSP00000416683.3:p.Ala49= | |
| ENST00000568221.1:c.65G>A (IGFALS) | ENSP00000456923.1:p.Arg22His | |
| ENST00000569769.1:c.-13+1252G>A (SPSB3) | ENSP00000455098.1:n.-13+1252G>A | |
| NM_001146006.1:c.147G>A (IGFALS) | NP_001139478.1:p.Ala49= | |
| NM_004970.2:c.33G>A (IGFALS) | NP_004961.1:p.Ala11= | |
| NR_027389.1:n.87G>A (IGFALS) | ||
| XM_011522476.1:c.114G>A (IGFALS) | XP_011520778.1:p.Ala38= | |
| NM_001146006.2:c.147G>A (IGFALS) | NP_001139478.1:p.Ala49= | |
| NM_004970.3:c.33G>A (IGFALS) MANE Select | NP_004961.1:p.Ala11= |