Linked Data
dbSNP Id:
rs767456657
ExAC:
1:11087532 C / G
gnomAD v2:
1-11087532-C-G
gnomAD v4:
1-11027475-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11027475C>G , CM000663.2:g.11027475C>G | GRCh38 |
| NC_000001.10:g.11087532C>G , CM000663.1:g.11087532C>G | GRCh37 |
| NC_000001.9:g.11010119C>G | NCBI36 |
| NG_007289.1:g.24754G>C | |
| NG_008734.1:g.19854C>G , LRG_659:g.19854C>G | |
| NG_007289.2:g.24754G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699927.1:n.410G>C (MASP2) | ||
| ENST00000699958.1:c.1366G>C (MASP2) | ENSP00000514717.1:p.Asp456His | |
| ENST00000700088.1:c.1298-627G>C (MASP2) | ENSP00000514787.1:n.1298-627G>C | |
| ENST00000700089.1:c.1468G>C (MASP2) | ENSP00000514788.1:n.1468G>C | |
| ENST00000700090.1:c.1350G>C (MASP2) | ENSP00000514789.1:n.1350G>C | |
| ENST00000700091.1:c.1273G>C (MASP2) | ENSP00000514790.1:p.Asp425His | |
| ENST00000700092.1:c.1450G>C (MASP2) | ENSP00000514791.1:p.Asp484His | |
| ENST00000700093.1:c.1447G>C (MASP2) | ENSP00000514792.1:p.Asp483His | |
| ENST00000700094.1:c.1479G>C (MASP2) | ENSP00000514793.1:n.1479G>C | |
| ENST00000700095.1:c.1298-627G>C (MASP2) | ENSP00000514794.1:n.1298-627G>C | |
| ENST00000700096.1:c.1101-627G>C (MASP2) | ENSP00000514795.1:n.1101-627G>C | |
| ENST00000700097.1:c.1499G>C (MASP2) | ENSP00000514796.1:n.1499G>C | |
| ENST00000400897.8:c.1471G>C (MASP2) MANE Select | ENSP00000383690.3:p.Asp491His | |
| ENST00000400897.7:c.1471G>C (MASP2) | ENSP00000383690.3:p.Asp491His | |
| ENST00000611136.4:c.448+2267C>G | ||
| ENST00000612542.1:c.206+2267C>G | ||
| ENST00000614757.4:c.*452+2267C>G | ENSP00000481867.1:n.*452+2267C>G | |
| ENST00000620028.1:n.416+2267C>G | ||
| ENST00000622108.1:c.232-2212C>G | ENSP00000480398.1:n.232-2212C>G | |
| NM_006610.3:c.1471G>C (MASP2) | NP_006601.2:p.Asp491His | |
| XM_017000863.2:c.*3011+1810C>G (TARDBP) | XP_016856352.1:n.*3011+1810C>G | |
| XM_017000864.2:c.*1895+1810C>G (TARDBP) | XP_016856353.1:n.*1895+1810C>G | |
| XM_017000865.2:c.*1781-2212C>G (TARDBP) | XP_016856354.1:n.*1781-2212C>G | |
| NM_006610.4:c.1471G>C (MASP2) MANE Select | NP_006601.2:p.Asp491His |