Linked Data
gnomAD v4:
20-6770400-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6770400T>A , CM000682.2:g.6770400T>A | GRCh38 |
| NC_000020.10:g.6751047T>A , CM000682.1:g.6751047T>A | GRCh37 |
| NC_000020.9:g.6699047T>A | NCBI36 |
| NG_023233.1:g.7303T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.274T>A MANE Select | ENSP00000368104.3:p.Ser92Thr | |
| ENST00000378827.4:c.274T>A | ENSP00000368104.3:p.Ser92Thr | |
| NM_001200.2:c.274T>A | NP_001191.1:p.Ser92Thr | |
| XM_011529323.1:c.-123+1525T>A | XP_011527625.1:n.-123+1525T>A | |
| NM_001200.3:c.274T>A | NP_001191.1:p.Ser92Thr | |
| NM_001200.4:c.274T>A MANE Select | NP_001191.1:p.Ser92Thr |