Linked Data
MyVariant Identifiers:
chr21:g.45708250A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44288367A>C , CM000683.2:g.44288367A>C | GRCh38 |
| NC_000021.8:g.45708250A>C , CM000683.1:g.45708250A>C | GRCh37 |
| NC_000021.7:g.44532678A>C | NCBI36 |
| NG_009556.1:g.7488A>C , LRG_18:g.7488A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.561A>C MANE Select | ENSP00000291582.5:p.Ser187= | |
| ENST00000291582.5:c.561A>C | ENSP00000291582.5:p.Ser187= | |
| ENST00000527919.5:n.1105A>C | ||
| ENST00000530812.5:n.1113A>C | ||
| NM_000383.3:c.561A>C | NP_000374.1:p.Ser187= | |
| XM_011529551.1:c.561A>C | XP_011527853.1:p.Ser187= | |
| NM_000383.4:c.561A>C MANE Select | NP_000374.1:p.Ser187= |