Linked Data
dbSNP Id:
rs909595427
gnomAD v2:
7-150648480-A-G
gnomAD v3:
7-150951392-A-G
gnomAD v4:
7-150951392-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150951392A>G , CM000669.2:g.150951392A>G | GRCh38 |
| NC_000007.13:g.150648480A>G , CM000669.1:g.150648480A>G | GRCh37 |
| NC_000007.12:g.150279413A>G | NCBI36 |
| NG_008916.1:g.31535T>C , LRG_288:g.31535T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.1243+56T>C | ||
| ENST00000683359.1:n.69+56T>C | ||
| ENST00000684241.1:n.2778+56T>C | ||
| ENST00000262186.10:c.1945+56T>C MANE Select | ENSP00000262186.5:n.1945+56T>C | |
| ENST00000330883.9:c.925+56T>C | ENSP00000328531.4:n.925+56T>C | |
| ENST00000262186.9:c.1945+56T>C | ENSP00000262186.5:n.1945+56T>C | |
| ENST00000330883.8:c.925+56T>C | ENSP00000328531.4:n.925+56T>C | |
| ENST00000430723.4:c.1597+56T>C | ENSP00000387657.4:n.1597+56T>C | |
| ENST00000461280.1:n.1232+56T>C | ||
| ENST00000473610.5:n.1306T>C | ||
| ENST00000532957.5:n.2168+56T>C | ||
| NM_000238.3:c.1945+56T>C , LRG_288t1:c.1945+56T>C | NP_000229.1:n.1945+56T>C | |
| NM_001204798.1:c.925+56T>C | NP_001191727.1:n.925+56T>C | |
| NM_172056.2:c.1945+56T>C , LRG_288t2:c.1945+56T>C | NP_742053.1:n.1945+56T>C | |
| NM_172057.2:c.925+56T>C , LRG_288t3:c.925+56T>C | NP_742054.1:n.925+56T>C | |
| XM_011516185.1:c.1645+56T>C | XP_011514487.1:n.1645+56T>C | |
| XM_011516186.1:c.1945+56T>C | XP_011514488.1:n.1945+56T>C | |
| XM_011516185.2:c.1645+56T>C | XP_011514487.1:n.1645+56T>C | |
| XM_011516186.3:c.1945+56T>C | XP_011514488.1:n.1945+56T>C | |
| XM_017012195.1:c.1795+56T>C | XP_016867684.1:n.1795+56T>C | |
| XM_017012196.1:c.1768+56T>C | XP_016867685.1:n.1768+56T>C | |
| NM_000238.4:c.1945+56T>C MANE Select | NP_000229.1:n.1945+56T>C | |
| NM_001204798.2:c.925+56T>C | NP_001191727.1:n.925+56T>C | |
| NM_172057.3:c.925+56T>C | NP_742054.1:n.925+56T>C |