Linked Data
ClinVar Variation Id:
165335
dbSNP Id:
rs727503455
ExAC:
17:37822159 G / A
gnomAD v2:
17-37822159-G-A
gnomAD v3:
17-39665906-G-A
gnomAD v4:
17-39665906-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665906G>A , CM000679.2:g.39665906G>A | GRCh38 |
| NC_000017.10:g.37822159G>A , CM000679.1:g.37822159G>A | GRCh37 |
| NC_000017.9:g.35075685G>A | NCBI36 |
| NG_008892.1:g.5561G>A , LRG_210:g.5561G>A | |
| NG_042278.1:g.2926G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.301G>A MANE Select | ENSP00000312624.2:p.Ala101Thr | |
| ENST00000309889.2:c.301G>A | ENSP00000312624.2:p.Ala101Thr | |
| ENST00000578283.1:c.229G>A | ENSP00000462787.1:p.Ala77Thr | |
| NM_003673.3:c.301G>A , LRG_210t1:c.301G>A | NP_003664.1:p.Ala101Thr | |
| NM_003673.4:c.301G>A MANE Select | NP_003664.1:p.Ala101Thr |