Linked Data
gnomAD v4:
6-31268829-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31268829A>T , CM000668.2:g.31268829A>T | GRCh38 |
| NC_000006.11:g.31236606A>T , CM000668.1:g.31236606A>T | GRCh37 |
| NC_000006.10:g.31344585A>T | NCBI36 |
| NG_029422.2:g.8303T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*340T>A MANE Select | ENSP00000365402.5:n.*340T>A | |
| ENST00000376228.9:c.*340T>A | ENSP00000365402.5:n.*340T>A | |
| ENST00000376237.8:c.*1028T>A | ENSP00000365412.4:n.*1028T>A | |
| ENST00000383329.7:c.*340T>A | ENSP00000372819.3:n.*340T>A | |
| ENST00000466892.5:n.674T>A | ||
| ENST00000470363.5:n.1199T>A | ||
| ENST00000487245.5:n.1800T>A | ||
| NM_002117.5:c.*340T>A | NP_002108.4:n.*340T>A | |
| NM_002117.6:c.*340T>A MANE Select | NP_002108.4:n.*340T>A |