Linked Data
ClinVar Variation Id:
627667
dbSNP Id:
rs761167679
ExAC:
7:150647231 C / A
gnomAD v2:
7-150647231-C-A
gnomAD v3:
7-150950143-C-A
gnomAD v4:
7-150950143-C-A
COSMIC:
COSM5976286
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150950143C>A , CM000669.2:g.150950143C>A | GRCh38 |
| NC_000007.13:g.150647231C>A , CM000669.1:g.150647231C>A | GRCh37 |
| NC_000007.12:g.150278164C>A | NCBI36 |
| NG_008916.1:g.32784G>T , LRG_288:g.32784G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461280.2:n.1721G>T | ||
| ENST00000684241.1:n.3231+25G>T | ||
| ENST00000262186.10:c.2398+25G>T MANE Select | ENSP00000262186.5:n.2398+25G>T | |
| ENST00000330883.9:c.1378+25G>T | ENSP00000328531.4:n.1378+25G>T | |
| ENST00000262186.9:c.2398+25G>T | ENSP00000262186.5:n.2398+25G>T | |
| ENST00000330883.8:c.1378+25G>T | ENSP00000328531.4:n.1378+25G>T | |
| ENST00000430723.4:c.2075G>T | ENSP00000387657.4:p.Gly692Val | |
| ENST00000461280.1:n.1710G>T | ||
| ENST00000473610.5:n.2055G>T | ||
| ENST00000532957.5:n.2646G>T | ||
| NM_000238.3:c.2398+25G>T , LRG_288t1:c.2398+25G>T | NP_000229.1:n.2398+25G>T | |
| NM_001204798.1:c.1403G>T | NP_001191727.1:p.Gly468Val | |
| NM_172056.2:c.2423G>T , LRG_288t2:c.2423G>T | NP_742053.1:p.Gly808Val | |
| NM_172057.2:c.1378+25G>T , LRG_288t3:c.1378+25G>T | NP_742054.1:n.1378+25G>T | |
| XM_011516185.1:c.2098+25G>T | XP_011514487.1:n.2098+25G>T | |
| XM_011516186.1:c.2398+25G>T | XP_011514488.1:n.2398+25G>T | |
| XM_011516185.2:c.2098+25G>T | XP_011514487.1:n.2098+25G>T | |
| XM_011516186.3:c.2398+25G>T | XP_011514488.1:n.2398+25G>T | |
| XM_017012195.1:c.2248+25G>T | XP_016867684.1:n.2248+25G>T | |
| XM_017012196.1:c.2221+25G>T | XP_016867685.1:n.2221+25G>T | |
| NM_000238.4:c.2398+25G>T MANE Select | NP_000229.1:n.2398+25G>T | |
| NM_001204798.2:c.1403G>T | NP_001191727.1:p.Gly468Val | |
| NM_172057.3:c.1378+25G>T | NP_742054.1:n.1378+25G>T |