Linked Data
gnomAD v4:
10-68231632-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231632C>T , CM000672.2:g.68231632C>T | GRCh38 |
| NC_000010.10:g.69991389C>T , CM000672.1:g.69991389C>T | GRCh37 |
| NC_000010.9:g.69661395C>T | NCBI36 |
| NG_031934.1:g.5482G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.46G>A MANE Select | ENSP00000362777.3:p.Ala16Thr | |
| ENST00000373673.4:c.46G>A | ENSP00000362777.3:p.Ala16Thr | |
| NM_145178.3:c.46G>A | NP_660161.1:p.Ala16Thr | |
| NM_145178.4:c.46G>A MANE Select | NP_660161.1:p.Ala16Thr |