Linked Data
ClinVar Variation Id:
236952
dbSNP Id:
rs878853626
gnomAD v2:
11-2906264-C-T
gnomAD v3:
11-2885034-C-T
gnomAD v4:
11-2885034-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2885034C>T , CM000673.2:g.2885034C>T | GRCh38 |
| NC_000011.9:g.2906264C>T , CM000673.1:g.2906264C>T | GRCh37 |
| NC_000011.8:g.2862840C>T | NCBI36 |
| NG_008022.1:g.5732G>A , LRG_533:g.5732G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681969.1:n.142+600G>A | ||
| ENST00000380725.2:c.255+168G>A | ENSP00000370101.1:n.255+168G>A | |
| ENST00000414822.8:c.456G>A | ENSP00000413720.3:p.Pro152= | |
| ENST00000430149.3:c.456G>A | ENSP00000411552.2:p.Pro152= | |
| ENST00000440480.8:c.423G>A MANE Select | ENSP00000411257.2:p.Pro141= | |
| ENST00000647251.1:c.255+168G>A | ENSP00000496631.1:n.255+168G>A | |
| ENST00000380725.1:c.255+168G>A | ENSP00000370101.1:n.255+168G>A | |
| ENST00000414822.7:c.456G>A | ENSP00000413720.3:p.Pro152= | |
| ENST00000430149.2:c.456G>A | ENSP00000411552.2:p.Pro152= | |
| ENST00000440480.6:c.423G>A | ENSP00000411257.2:p.Pro141= | |
| NM_000076.2:c.456G>A , LRG_533t1:c.456G>A | NP_000067.1:p.Pro152= | |
| NM_001122630.1:c.423G>A | NP_001116102.1:p.Pro141= | |
| NM_001122631.1:c.423G>A | NP_001116103.1:p.Pro141= | |
| XM_005252732.3:c.255+168G>A | XP_005252789.1:n.255+168G>A | |
| NM_001362474.1:c.456G>A | NP_001349403.1:p.Pro152= | |
| NM_001362475.1:c.255+168G>A | NP_001349404.1:n.255+168G>A | |
| NM_001122630.2:c.423G>A MANE Select | NP_001116102.1:p.Pro141= | |
| NM_001122631.2:c.423G>A | NP_001116103.1:p.Pro141= | |
| NM_001362474.2:c.456G>A | NP_001349403.1:p.Pro152= | |
| NM_001362475.2:c.255+168G>A | NP_001349404.1:n.255+168G>A |