Linked Data
ClinVar Variation Id:
338317
dbSNP Id:
rs748907807
ExAC:
20:34022109 G / A
gnomAD v2:
20-34022109-G-A
gnomAD v3:
20-35434311-G-A
gnomAD v4:
20-35434311-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35434311G>A , CM000682.2:g.35434311G>A | GRCh38 |
| NC_000020.10:g.34022109G>A , CM000682.1:g.34022109G>A | GRCh37 |
| NC_000020.9:g.33485523G>A | NCBI36 |
| NG_008076.2:g.8909C>T | |
| NG_008076.3:g.25436C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374369.8:c.1104C>T (GDF5) MANE Select | ENSP00000363489.3:p.Thr368= | |
| ENST00000374369.7:c.1104C>T (GDF5) | ENSP00000363489.3:p.Thr368= | |
| ENST00000374372.1:c.1104C>T (GDF5) | ENSP00000363492.1:p.Thr368= | |
| ENST00000374375.1:c.153G>A (GDF5-AS1) | ENSP00000363495.1:p.Thr51= | |
| NM_000557.4:c.1104C>T (GDF5) | NP_000548.2:p.Thr368= | |
| XM_011529075.1:c.1104C>T (GDF5) | XP_011527377.1:p.Thr368= | |
| XM_011529076.1:c.1104C>T (GDF5) | XP_011527378.1:p.Thr368= | |
| NM_001319138.1:c.1104C>T (GDF5) | NP_001306067.1:p.Thr368= | |
| NM_001355428.1:c.153G>A (GDF5-AS1) | NP_001342357.1:p.Thr51= | |
| NM_000557.5:c.1104C>T (GDF5) MANE Select | NP_000548.2:p.Thr368= | |
| NM_001319138.2:c.1104C>T (GDF5) | NP_001306067.1:p.Thr368= | |
| NR_161326.1:n.595G>A (GDF5-AS1) |