Linked Data
gnomAD v4:
6-31270063-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270063G>C , CM000668.2:g.31270063G>C | GRCh38 |
| NC_000006.11:g.31237840G>C , CM000668.1:g.31237840G>C | GRCh37 |
| NC_000006.10:g.31345819G>C | NCBI36 |
| NG_029422.2:g.7069C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.918C>G MANE Select | ENSP00000365402.5:p.Ile306Met | |
| ENST00000376228.9:c.918C>G | ENSP00000365402.5:p.Ile306Met | |
| ENST00000376237.8:c.*505C>G | ENSP00000365412.4:n.*505C>G | |
| ENST00000383329.7:c.918C>G | ENSP00000372819.3:p.Ile306Met | |
| ENST00000470363.5:n.236C>G | ||
| ENST00000487245.5:n.1277C>G | ||
| NM_002117.5:c.918C>G | NP_002108.4:p.Ile306Met | |
| NM_002117.6:c.918C>G MANE Select | NP_002108.4:p.Ile306Met |