Linked Data
gnomAD v4:
10-103458361-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458361T>C , CM000672.2:g.103458361T>C | GRCh38 |
| NC_000010.10:g.105218118T>C , CM000672.1:g.105218118T>C | GRCh37 |
| NC_000010.9:g.105208108T>C | NCBI36 |
| NG_016855.1:g.5531A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329905.6:c.391A>G MANE Select | ENSP00000329926.6:p.Thr131Ala | |
| ENST00000329905.5:c.391A>G | ENSP00000329926.5:p.Thr131Ala | |
| NM_001001412.3:c.391A>G | NP_001001412.3:p.Thr131Ala | |
| NM_001001412.4:c.391A>G MANE Select | NP_001001412.3:p.Thr131Ala |