Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94031104G>T , CM000663.2:g.94031104G>T | GRCh38 |
| NC_000001.10:g.94496660G>T , CM000663.1:g.94496660G>T | GRCh37 |
| NC_000001.9:g.94269248G>T | NCBI36 |
| NG_009073.1:g.95046C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4145C>A MANE Select | ENSP00000359245.3:p.Thr1382Asn | |
| ENST00000370225.3:c.4145C>A | ENSP00000359245.3:p.Thr1382Asn | |
| ENST00000536513.5:c.521C>A | ENSP00000439707.2:p.Thr174Asn | |
| NM_000350.2:c.4145C>A | NP_000341.2:p.Thr1382Asn | |
| NM_000350.3:c.4145C>A MANE Select | NP_000341.2:p.Thr1382Asn |