Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667367A>T , CM000683.2:g.31667367A>T | GRCh38 |
| NC_000021.8:g.33039680A>T , CM000683.1:g.33039680A>T | GRCh37 |
| NC_000021.7:g.31961551A>T | NCBI36 |
| NG_008689.1:g.12746A>T , LRG_652:g.12746A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.349A>T MANE Select | ENSP00000270142.7:p.Thr117Ser | |
| ENST00000270142.10:c.349A>T | ENSP00000270142.6:p.Thr117Ser | |
| ENST00000389995.4:c.292A>T | ENSP00000374645.4:p.Thr98Ser | |
| ENST00000470944.1:n.1277A>T | ||
| NM_000454.4:c.349A>T , LRG_652t1:c.349A>T | NP_000445.1:p.Thr117Ser | |
| NM_000454.5:c.349A>T MANE Select | NP_000445.1:p.Thr117Ser |