Linked Data
dbSNP Id:
rs561663073
gnomAD v2:
7-107560599-A-G
gnomAD v3:
7-107920154-A-G
gnomAD v4:
7-107920154-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107920154A>G , CM000669.2:g.107920154A>G | GRCh38 |
| NC_000007.13:g.107560599A>G , CM000669.1:g.107560599A>G | GRCh37 |
| NC_000007.12:g.107347835A>G | NCBI36 |
| NG_008045.1:g.34014A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205402.10:c.*895A>G MANE Select | ENSP00000205402.3:n.*895A>G | |
| ENST00000205402.9:c.*895A>G | ENSP00000205402.3:n.*895A>G | |
| ENST00000417551.5:c.*124+771A>G | ENSP00000390667.1:n.*124+771A>G | |
| NM_000108.4:c.*895A>G | NP_000099.2:n.*895A>G | |
| NM_001289750.1:c.*895A>G | NP_001276679.1:n.*895A>G | |
| NM_001289751.1:c.*895A>G | NP_001276680.1:n.*895A>G | |
| NM_001289752.1:c.*895A>G | NP_001276681.1:n.*895A>G | |
| NM_000108.5:c.*895A>G MANE Select | NP_000099.2:n.*895A>G |