Linked Data
gnomAD v4:
5-1213629-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213629T>G , CM000667.2:g.1213629T>G | GRCh38 |
| NC_000005.9:g.1213744T>G , CM000667.1:g.1213744T>G | GRCh37 |
| NC_000005.8:g.1266744T>G | NCBI36 |
| NG_008282.1:g.17035T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.774+56T>G MANE Select | ENSP00000305302.10:n.774+56T>G | |
| ENST00000304460.10:c.774+56T>G | ENSP00000305302.10:n.774+56T>G | |
| ENST00000515652.5:c.682+56T>G | ENSP00000425701.1:n.682+56T>G | |
| NM_001003841.2:c.774+56T>G | NP_001003841.1:n.774+56T>G | |
| NM_001003841.3:c.774+56T>G MANE Select | NP_001003841.1:n.774+56T>G |