Linked Data
ClinVar Variation Id:
1588921
ClinVar RCV Id:
RCV002098578
dbSNP Id:
rs945006442
gnomAD v4:
16-28937126-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28937126G>A , CM000678.2:g.28937126G>A | GRCh38 |
| NC_000016.9:g.28948447G>A , CM000678.1:g.28948447G>A | GRCh37 |
| NC_000016.8:g.28855948G>A | NCBI36 |
| NG_007275.1:g.10188G>A , LRG_35:g.10188G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324662.8:c.1188G>A | ENSP00000313419.4:p.Pro396= | |
| ENST00000538922.8:c.1188G>A MANE Select | ENSP00000437940.2:p.Pro396= | |
| ENST00000324662.7:c.1188G>A | ENSP00000313419.3:p.Pro396= | |
| ENST00000538922.5:c.1188G>A | ENSP00000437940.1:p.Pro396= | |
| ENST00000565089.5:n.1522G>A | ||
| ENST00000567368.1:n.328G>A | ||
| ENST00000567541.5:c.1188G>A | ENSP00000456201.1:p.Pro396= | |
| ENST00000611258.4:c.1187G>A | ENSP00000481090.1:p.Arg396His | |
| NM_001178098.1:c.1188G>A | NP_001171569.1:p.Pro396= | |
| NM_001770.5:c.1188G>A , LRG_35t1:c.1188G>A | NP_001761.3:p.Pro396= | |
| XM_006721103.2:c.921G>A | XP_006721166.1:p.Pro307= | |
| XM_006721103.3:c.921G>A | XP_006721166.1:p.Pro307= | |
| XM_017023893.1:c.921G>A | XP_016879382.1:p.Pro307= | |
| NM_001178098.2:c.1188G>A | NP_001171569.1:p.Pro396= | |
| NM_001770.6:c.1188G>A MANE Select | NP_001761.3:p.Pro396= | |
| NM_001385732.1:c.921G>A | NP_001372661.1:p.Pro307= | |
| NR_169755.1:n.1530G>A |