Linked Data
MyVariant Identifiers:
chr21:g.33039598T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667285T>G , CM000683.2:g.31667285T>G | GRCh38 |
| NC_000021.8:g.33039598T>G , CM000683.1:g.33039598T>G | GRCh37 |
| NC_000021.7:g.31961469T>G | NCBI36 |
| NG_008689.1:g.12664T>G , LRG_652:g.12664T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.267T>G MANE Select | ENSP00000270142.7:p.Thr89= | |
| ENST00000270142.10:c.267T>G | ENSP00000270142.6:p.Thr89= | |
| ENST00000389995.4:c.210T>G | ENSP00000374645.4:p.Thr70= | |
| ENST00000470944.1:n.1195T>G | ||
| ENST00000476106.5:n.530T>G | ||
| NM_000454.4:c.267T>G , LRG_652t1:c.267T>G | NP_000445.1:p.Thr89= | |
| NM_000454.5:c.267T>G MANE Select | NP_000445.1:p.Thr89= |