Linked Data
gnomAD v3:
6-31271645-T-C
gnomAD v4:
6-31271645-T-C
MyVariant Identifiers:
chr6:g.31239422T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271645T>C , CM000668.2:g.31271645T>C | GRCh38 |
| NC_000006.11:g.31239422T>C , CM000668.1:g.31239422T>C | GRCh37 |
| NC_000006.10:g.31347401T>C | NCBI36 |
| NG_029422.2:g.5487A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.297A>G MANE Select | ENSP00000365402.5:p.Arg99= | |
| ENST00000376228.9:c.297A>G | ENSP00000365402.5:p.Arg99= | |
| ENST00000376237.8:c.297A>G | ENSP00000365412.4:p.Arg99= | |
| ENST00000383329.7:c.297A>G | ENSP00000372819.3:p.Arg99= | |
| ENST00000415537.1:c.295A>G | ||
| ENST00000484378.1:n.316A>G | ||
| ENST00000487245.5:n.406A>G | ||
| ENST00000495835.1:n.486A>G | ||
| NM_002117.5:c.297A>G | NP_002108.4:p.Arg99= | |
| NM_002117.6:c.297A>G MANE Select | NP_002108.4:p.Arg99= |