Linked Data
ClinVar Variation Id:
2714687
ClinVar RCV Id:
RCV003496488
dbSNP Id:
rs1398558607
gnomAD v3:
11-61393950-G-T
gnomAD v4:
11-61393950-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61393950G>T , CM000673.2:g.61393950G>T | GRCh38 |
| NC_000011.9:g.61161422G>T , CM000673.1:g.61161422G>T | GRCh37 |
| NC_000011.8:g.60917998G>T | NCBI36 |
| NG_032976.1:g.6591G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.10:c.203G>T | ENSP00000334844.5:p.Gly68Val | |
| ENST00000544795.6:n.480G>T | ||
| ENST00000684926.1:n.219G>T | ||
| ENST00000688959.1:c.-57G>T | ENSP00000509213.1:n.-57G>T | |
| ENST00000690736.1:c.203G>T | ENSP00000508542.1:p.Gly68Val | |
| ENST00000515837.7:c.203G>T MANE Select | ENSP00000440638.1:p.Gly68Val | |
| ENST00000334888.9:c.203G>T | ENSP00000334844.5:p.Gly68Val | |
| ENST00000398979.7:c.20G>T | ENSP00000381950.3:p.Gly7Val | |
| ENST00000515837.6:c.203G>T | ENSP00000440638.1:p.Gly68Val | |
| ENST00000541473.1:n.217G>T | ||
| ENST00000544795.5:n.219G>T | ||
| NM_001173990.2:c.203G>T | NP_001167461.1:p.Gly68Val | |
| NM_001173991.2:c.203G>T | NP_001167462.1:p.Gly68Val | |
| NM_016499.5:c.20G>T | NP_057583.2:p.Gly7Val | |
| XM_005274039.3:c.20G>T | XP_005274096.1:p.Gly7Val | |
| NM_001330285.1:c.20G>T | NP_001317214.1:p.Gly7Val | |
| XM_005274039.4:c.20G>T | XP_005274096.1:p.Gly7Val | |
| NM_001173990.3:c.203G>T MANE Select | NP_001167461.1:p.Gly68Val | |
| NM_001173991.3:c.203G>T | NP_001167462.1:p.Gly68Val | |
| NM_001330285.2:c.20G>T | NP_001317214.1:p.Gly7Val | |
| NM_016499.6:c.20G>T | NP_057583.2:p.Gly7Val |