Linked Data
MyVariant Identifiers:
chr21:g.47410315C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990401C>A , CM000683.2:g.45990401C>A | GRCh38 |
| NC_000021.8:g.47410315C>A , CM000683.1:g.47410315C>A | GRCh37 |
| NC_000021.7:g.46234743C>A | NCBI36 |
| NG_008674.1:g.13653C>A , LRG_475:g.13653C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.981C>A MANE Select | ENSP00000355180.3:p.Ile327= | |
| ENST00000361866.7:c.981C>A | ENSP00000355180.3:p.Ile327= | |
| ENST00000612273.1:c.981C>A | ENSP00000483630.1:p.Ile327= | |
| NM_001848.2:c.981C>A , LRG_475t1:c.981C>A | NP_001839.2:p.Ile327= | |
| NM_001848.3:c.981C>A MANE Select | NP_001839.2:p.Ile327= |