Linked Data
MyVariant Identifiers:
chr21:g.45706523A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44286640A>T , CM000683.2:g.44286640A>T | GRCh38 |
| NC_000021.8:g.45706523A>T , CM000683.1:g.45706523A>T | GRCh37 |
| NC_000021.7:g.44530951A>T | NCBI36 |
| NG_009556.1:g.5761A>T , LRG_18:g.5761A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.216A>T MANE Select | ENSP00000291582.5:p.Thr72= | |
| ENST00000291582.5:c.216A>T | ENSP00000291582.5:p.Thr72= | |
| ENST00000527919.5:n.377A>T | ||
| ENST00000530812.5:n.385A>T | ||
| NM_000383.3:c.216A>T | NP_000374.1:p.Thr72= | |
| XM_011529551.1:c.216A>T | XP_011527853.1:p.Thr72= | |
| NM_000383.4:c.216A>T MANE Select | NP_000374.1:p.Thr72= |