Linked Data
MyVariant Identifiers:
chr21:g.45194092G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43774211G>C , CM000683.2:g.43774211G>C | GRCh38 |
| NC_000021.8:g.45194092G>C , CM000683.1:g.45194092G>C | GRCh37 |
| NC_000021.7:g.44018520G>C | NCBI36 |
| NG_011545.1:g.7168C>G , LRG_485:g.7168C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291568.7:c.288C>G MANE Select | ENSP00000291568.6:p.Thr96= | |
| ENST00000480147.3:n.2058C>G | ||
| ENST00000639959.1:c.155C>G | ||
| ENST00000640406.1:c.*363C>G | ENSP00000492672.1:n.*363C>G | |
| ENST00000675996.1:n.713C>G | ||
| ENST00000291568.5:c.288C>G | ENSP00000291568.5:p.Thr96= | |
| ENST00000480147.1:n.652C>G | ||
| NM_000100.3:c.288C>G , LRG_485t1:c.288C>G | NP_000091.1:p.Thr96= | |
| NM_000100.4:c.288C>G MANE Select | NP_000091.1:p.Thr96= |