Linked Data
gnomAD v4:
6-31270323-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270323C>G , CM000668.2:g.31270323C>G | GRCh38 |
| NC_000006.11:g.31238100C>G , CM000668.1:g.31238100C>G | GRCh37 |
| NC_000006.10:g.31346079C>G | NCBI36 |
| NG_029422.2:g.6809G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.782G>C MANE Select | ENSP00000365402.5:p.Gly261Ala | |
| ENST00000376228.9:c.782G>C | ENSP00000365402.5:p.Gly261Ala | |
| ENST00000376237.8:c.*369G>C | ENSP00000365412.4:n.*369G>C | |
| ENST00000383329.7:c.782G>C | ENSP00000372819.3:p.Gly261Ala | |
| ENST00000415537.1:c.673G>C | ||
| ENST00000470363.5:n.100G>C | ||
| ENST00000487245.5:n.1141G>C | ||
| ENST00000495835.1:n.971G>C | ||
| NM_002117.5:c.782G>C | NP_002108.4:p.Gly261Ala | |
| NM_002117.6:c.782G>C MANE Select | NP_002108.4:p.Gly261Ala |