Linked Data
gnomAD v4:
11-299462-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.299462G>C , CM000673.2:g.299462G>C | GRCh38 |
| NC_000011.9:g.299462G>C , CM000673.1:g.299462G>C | GRCh37 |
| NC_000011.8:g.289462G>C | NCBI36 |
| NG_032892.1:g.5065C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382614.2:c.29C>G MANE Select | ENSP00000372059.2:p.Thr10Ser | |
| NM_001025295.2:c.29C>G | NP_001020466.1:p.Thr10Ser | |
| NM_001025295.3:c.29C>G MANE Select | NP_001020466.1:p.Thr10Ser |