Linked Data
MyVariant Identifiers:
chr21:g.47421192C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46001278C>G , CM000683.2:g.46001278C>G | GRCh38 |
| NC_000021.8:g.47421192C>G , CM000683.1:g.47421192C>G | GRCh37 |
| NC_000021.7:g.46245620C>G | NCBI36 |
| NG_008674.1:g.24530C>G , LRG_475:g.24530C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463060.6:n.247C>G | ||
| ENST00000361866.8:c.1848C>G MANE Select | ENSP00000355180.3:p.Leu616= | |
| ENST00000361866.7:c.1848C>G | ENSP00000355180.3:p.Leu616= | |
| ENST00000463060.5:n.247C>G | ||
| ENST00000498614.5:n.82C>G | ||
| ENST00000612273.1:c.1842C>G | ENSP00000483630.1:p.Leu614= | |
| NM_001848.2:c.1848C>G , LRG_475t1:c.1848C>G | NP_001839.2:p.Leu616= | |
| NM_001848.3:c.1848C>G MANE Select | NP_001839.2:p.Leu616= |