Linked Data
gnomAD v4:
6-31269029-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269029C>A , CM000668.2:g.31269029C>A | GRCh38 |
| NC_000006.11:g.31236806C>A , CM000668.1:g.31236806C>A | GRCh37 |
| NC_000006.10:g.31344785C>A | NCBI36 |
| NG_029422.2:g.8103G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*140G>T MANE Select | ENSP00000365402.5:n.*140G>T | |
| ENST00000376228.9:c.*140G>T | ENSP00000365402.5:n.*140G>T | |
| ENST00000376237.8:c.*828G>T | ENSP00000365412.4:n.*828G>T | |
| ENST00000383329.7:c.*140G>T | ENSP00000372819.3:n.*140G>T | |
| ENST00000466892.5:n.474G>T | ||
| ENST00000470363.5:n.999G>T | ||
| ENST00000487245.5:n.1600G>T | ||
| NM_002117.5:c.*140G>T | NP_002108.4:n.*140G>T | |
| NM_002117.6:c.*140G>T MANE Select | NP_002108.4:n.*140G>T |