Linked Data
dbSNP Id:
rs770854110
ExAC:
7:143028024 A / G
gnomAD v2:
7-143028024-A-G
gnomAD v4:
7-143330931-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143330931A>G , CM000669.2:g.143330931A>G | GRCh38 |
| NC_000007.13:g.143028024A>G , CM000669.1:g.143028024A>G | GRCh37 |
| NC_000007.12:g.142738146A>G | NCBI36 |
| NG_009815.1:g.19806A>G | |
| NG_009815.2:g.19806A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.979+34A>G | ENSP00000498052.2:n.979+34A>G | |
| ENST00000343257.7:c.979+34A>G MANE Select | ENSP00000339867.2:n.979+34A>G | |
| ENST00000432192.6:c.803+34A>G | ||
| ENST00000343257.6:c.979+34A>G | ENSP00000339867.2:n.979+34A>G | |
| NM_000083.2:c.979+34A>G | NP_000074.2:n.979+34A>G | |
| NR_046453.1:n.1069+34A>G | ||
| XM_011515781.1:c.979+34A>G | XP_011514083.1:n.979+34A>G | |
| XM_017011739.1:c.529+34A>G | XP_016867228.1:n.529+34A>G | |
| XM_017011740.1:c.529+34A>G | XP_016867229.1:n.529+34A>G | |
| NM_000083.3:c.979+34A>G MANE Select | NP_000074.3:n.979+34A>G | |
| NR_046453.2:n.1084+34A>G |