Linked Data
ClinVar Variation Id:
1576234
ClinVar RCV Id:
RCV002085280
dbSNP Id:
rs773263009
ExAC:
11:45827505 C / G
gnomAD v2:
11-45827505-C-G
gnomAD v3:
11-45805954-C-G
gnomAD v4:
11-45805954-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.45805954C>G , CM000673.2:g.45805954C>G | GRCh38 |
| NC_000011.9:g.45827505C>G , CM000673.1:g.45827505C>G | GRCh37 |
| NC_000011.8:g.45784081C>G | NCBI36 |
| NG_009875.1:g.6883C>G , LRG_107:g.6883C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526817.2:c.114C>G | ENSP00000432145.2:p.Thr38= | |
| ENST00000314134.4:c.153C>G MANE Select | ENSP00000313318.3:p.Thr51= | |
| ENST00000314134.3:c.153C>G | ENSP00000313318.3:p.Thr51= | |
| ENST00000442528.2:c.114C>G | ENSP00000412408.2:p.Thr38= | |
| ENST00000526817.1:c.114C>G | ENSP00000432145.1:p.Thr38= | |
| ENST00000530471.1:c.114C>G | ENSP00000432669.1:p.Thr38= | |
| NM_001145265.1:c.114C>G | NP_001138737.1:p.Thr38= | |
| NM_001145266.1:c.114C>G | NP_001138738.1:p.Thr38= | |
| NM_018389.4:c.153C>G , LRG_107t1:c.153C>G | NP_060859.4:p.Thr51= | |
| XM_011520203.1:c.153C>G | XP_011518505.1:p.Thr51= | |
| XM_011520203.3:c.153C>G | XP_011518505.1:p.Thr51= | |
| NM_001145265.2:c.114C>G | NP_001138737.1:p.Thr38= | |
| NM_018389.5:c.153C>G MANE Select | NP_060859.4:p.Thr51= |