Linked Data
MyVariant Identifiers:
chr21:g.43176778C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41756618C>T , CM000683.2:g.41756618C>T | GRCh38 |
| NC_000021.8:g.43176778C>T , CM000683.1:g.43176778C>T | GRCh37 |
| NC_000021.7:g.42049847C>T | NCBI36 |
| NG_032113.1:g.15472G>A | |
| NG_032113.2:g.15472G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332512.8:c.381G>A MANE Select | ENSP00000332454.3:p.Val127= | |
| ENST00000332512.7:c.381G>A | ENSP00000332454.3:p.Val127= | |
| ENST00000352483.3:c.381G>A | ENSP00000330161.2:p.Val127= | |
| NM_020639.2:c.381G>A | NP_065690.2:p.Val127= | |
| NM_020639.3:c.381G>A MANE Select | NP_065690.2:p.Val127= |