Linked Data
gnomAD v4:
17-4631995-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4631995G>T , CM000679.2:g.4631995G>T | GRCh38 |
| NC_000017.10:g.4535290G>T , CM000679.1:g.4535290G>T | GRCh37 |
| NC_000017.9:g.4482039G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293761.8:c.1703C>A MANE Select | ENSP00000293761.3:p.Thr568Asn | |
| ENST00000570836.6:c.1703C>A | ENSP00000458832.1:p.Thr568Asn | |
| ENST00000293761.7:c.1703C>A | ENSP00000293761.3:p.Thr568Asn | |
| ENST00000570836.5:c.1703C>A | ENSP00000458832.1:p.Thr568Asn | |
| ENST00000574640.1:c.1586C>A | ENSP00000460483.1:p.Thr529Asn | |
| NM_001140.3:c.1703C>A | NP_001131.3:p.Thr568Asn | |
| NM_001140.4:c.1703C>A | NP_001131.3:p.Thr568Asn | |
| NM_001140.5:c.1703C>A MANE Select | NP_001131.3:p.Thr568Asn |