Linked Data
MyVariant Identifiers:
chr21:g.45708262T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44288379T>C , CM000683.2:g.44288379T>C | GRCh38 |
| NC_000021.8:g.45708262T>C , CM000683.1:g.45708262T>C | GRCh37 |
| NC_000021.7:g.44532690T>C | NCBI36 |
| NG_009556.1:g.7500T>C , LRG_18:g.7500T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.573T>C MANE Select | ENSP00000291582.5:p.Ala191= | |
| ENST00000291582.5:c.573T>C | ENSP00000291582.5:p.Ala191= | |
| ENST00000527919.5:n.1117T>C | ||
| ENST00000530812.5:n.1125T>C | ||
| NM_000383.3:c.573T>C | NP_000374.1:p.Ala191= | |
| XM_011529551.1:c.573T>C | XP_011527853.1:p.Ala191= | |
| NM_000383.4:c.573T>C MANE Select | NP_000374.1:p.Ala191= |