Linked Data
gnomAD v4:
7-107701974-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107701974C>T , CM000669.2:g.107701974C>T | GRCh38 |
| NC_000007.13:g.107342419C>T , CM000669.1:g.107342419C>T | GRCh37 |
| NC_000007.12:g.107129655C>T | NCBI36 |
| NG_008489.1:g.46340C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644269.2:c.1951C>T MANE Select | ENSP00000494017.1:p.Pro651Ser | |
| ENST00000644846.1:c.662C>T | ||
| ENST00000265715.7:c.1951C>T | ENSP00000265715.3:p.Pro651Ser | |
| ENST00000492030.2:n.238C>T | ||
| NM_000441.1:c.1951C>T | NP_000432.1:p.Pro651Ser | |
| XM_005250425.1:c.1951C>T | XP_005250482.1:p.Pro651Ser | |
| XM_005250425.2:c.1951C>T | XP_005250482.1:p.Pro651Ser | |
| XM_017012318.1:c.1873C>T | XP_016867807.1:p.Pro625Ser | |
| NM_000441.2:c.1951C>T MANE Select | NP_000432.1:p.Pro651Ser |