Linked Data
ClinVar Variation Id:
751220
dbSNP Id:
rs137930991
ExAC:
22:50967962 G / A
gnomAD v2:
22-50967962-G-A
gnomAD v3:
22-50529533-G-A
gnomAD v4:
22-50529533-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50529533G>A , CM000684.2:g.50529533G>A | GRCh38 |
| NC_000022.10:g.50967962G>A , CM000684.1:g.50967962G>A | GRCh37 |
| NC_000022.9:g.49314828G>A | NCBI36 |
| NG_011860.1:g.5553C>T , LRG_727:g.5553C>T | |
| NG_016235.1:g.1907C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252029.8:c.177C>T MANE Select | ENSP00000252029.3:p.Ala59= | |
| ENST00000395680.6:c.177C>T | ENSP00000379037.1:p.Ala59= | |
| ENST00000395681.6:c.177C>T | ENSP00000379038.1:p.Ala59= | |
| ENST00000650719.1:c.177C>T | ENSP00000498276.1:p.Ala59= | |
| ENST00000651095.1:n.316C>T | ||
| ENST00000651196.1:c.177C>T | ENSP00000499096.1:p.Ala59= | |
| ENST00000651401.1:c.-1+371C>T | ENSP00000499115.1:n.-1+371C>T | |
| ENST00000651906.1:n.296C>T | ||
| ENST00000652237.1:n.296C>T | ||
| ENST00000252029.7:c.177C>T | ENSP00000252029.3:p.Ala59= | |
| ENST00000395678.7:c.177C>T | ENSP00000379036.3:p.Ala59= | |
| ENST00000395680.5:c.177C>T | ENSP00000379037.1:p.Ala59= | |
| ENST00000395681.5:c.177C>T | ENSP00000379038.1:p.Ala59= | |
| ENST00000425169.1:c.177C>T | ENSP00000395875.1:p.Ala59= | |
| ENST00000476284.1:n.302C>T | ||
| ENST00000487162.1:n.308C>T | ||
| ENST00000487577.5:n.464C>T | ||
| NM_001113755.2:c.177C>T | NP_001107227.1:p.Ala59= | |
| NM_001113756.2:c.177C>T | NP_001107228.1:p.Ala59= | |
| NM_001257988.1:c.177C>T , LRG_727t1:c.177C>T | NP_001244917.1:p.Ala59= | |
| NM_001257989.1:c.177C>T , LRG_727t2:c.177C>T | NP_001244918.1:p.Ala59= | |
| NM_001953.4:c.177C>T | NP_001944.1:p.Ala59= | |
| NM_001113755.3:c.177C>T | NP_001107227.1:p.Ala59= | |
| NM_001113756.3:c.177C>T | NP_001107228.1:p.Ala59= | |
| NM_001953.5:c.177C>T MANE Select | NP_001944.1:p.Ala59= |