Linked Data
MyVariant Identifiers:
chr21:g.43172114G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43172114G>C , CM000683.2:g.43172114G>C | GRCh38 |
| NG_009823.1:g.8084G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.356G>C MANE Select | ENSP00000291554.2:p.Arg119Pro | |
| ENST00000398132.1:c.245G>C | ENSP00000381200.1:p.Arg82Pro | |
| ENST00000398133.5:c.296G>C | ENSP00000381201.1:p.Arg99Pro | |
| ENST00000468016.1:n.457G>C | ||
| ENST00000482775.1:n.437G>C | ||
| NM_000394.3:c.356G>C | NP_000385.1:p.Arg119Pro | |
| XM_005261093.2:c.245G>C | XP_005261150.1:p.Arg82Pro | |
| NM_001363766.1:c.245G>C | NP_001350695.1:p.Arg82Pro | |
| NM_000394.4:c.356G>C MANE Select | NP_000385.1:p.Arg119Pro |