Linked Data
dbSNP Id:
rs758910665
gnomAD v2:
5-136974669-C-T
gnomAD v3:
5-137638980-C-T
gnomAD v4:
5-137638980-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.137638980C>T , CM000667.2:g.137638980C>T | GRCh38 |
| NC_000005.9:g.136974669C>T , CM000667.1:g.136974669C>T | GRCh37 |
| NC_000005.8:g.137002568C>T | NCBI36 |
| NG_032569.1:g.102111G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309755.9:c.1192G>A MANE Select | ENSP00000312397.4:p.Ala398Thr | |
| ENST00000309755.8:c.1192G>A | ENSP00000312397.4:p.Ala398Thr | |
| ENST00000502381.1:n.779G>A | ||
| ENST00000504208.5:c.*335-10543G>A | ENSP00000423585.1:n.*335-10543G>A | |
| ENST00000505853.1:c.1072G>A | ENSP00000426173.1:p.Ala358Thr | |
| ENST00000506491.5:c.946G>A | ENSP00000424828.1:p.Ala316Thr | |
| ENST00000506873.5:n.817G>A | ||
| ENST00000508657.5:c.1096G>A | ENSP00000422099.1:p.Ala366Thr | |
| NM_001257194.1:c.1096G>A | NP_001244123.1:p.Ala366Thr | |
| NM_001257195.1:c.946G>A | NP_001244124.1:p.Ala316Thr | |
| NM_017415.2:c.1192G>A | NP_059111.2:p.Ala398Thr | |
| NM_017415.3:c.1192G>A MANE Select | NP_059111.2:p.Ala398Thr | |
| NM_001257195.2:c.946G>A | NP_001244124.1:p.Ala316Thr |