Linked Data
gnomAD v4:
11-124872956-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872956T>C , CM000673.2:g.124872956T>C | GRCh38 |
| NC_000011.9:g.124742852T>C , CM000673.1:g.124742852T>C | GRCh37 |
| NC_000011.8:g.124248062T>C | NCBI36 |
| NG_016214.1:g.12548T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1403T>C MANE Select | ENSP00000380903.1:p.Val468Ala | |
| ENST00000397801.5:c.1403T>C | ENSP00000380903.1:p.Val468Ala | |
| ENST00000538940.5:c.1337T>C | ENSP00000441797.1:p.Val446Ala | |
| NM_022370.3:c.1403T>C | NP_071765.2:p.Val468Ala | |
| XM_011542953.1:c.2375T>C | XP_011541255.1:p.Val792Ala | |
| XM_017018122.1:c.1337T>C | XP_016873611.1:p.Val446Ala | |
| NM_022370.4:c.1403T>C MANE Select | NP_071765.2:p.Val468Ala |