Linked Data
ClinVar Variation Id:
236448
dbSNP Id:
rs878853350
gnomAD v3:
6-64307024-C-T
gnomAD v4:
6-64307024-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.64307024C>T , CM000668.2:g.64307024C>T | GRCh38 |
| NC_000006.11:g.65016917C>T , CM000668.1:g.65016917C>T | GRCh37 |
| NC_000006.10:g.65074876C>T | NCBI36 |
| NG_023443.1:g.1405202G>A | |
| NG_023443.2:g.1405202G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.6137G>A MANE Select | ENSP00000424243.1:p.Trp2046Ter | |
| ENST00000370616.6:c.6137G>A | ENSP00000359650.2:p.Trp2046Ter | |
| ENST00000370618.7:c.6137G>A | ENSP00000359652.4:p.Trp2046Ter | |
| ENST00000370621.7:c.6137G>A | ENSP00000359655.3:p.Trp2046Ter | |
| ENST00000503581.5:c.6137G>A | ENSP00000424243.1:p.Trp2046Ter | |
| NM_001142800.1:c.6137G>A | NP_001136272.1:p.Trp2046Ter | |
| NM_001292009.1:c.6137G>A | NP_001278938.1:p.Trp2046Ter | |
| NM_001142800.2:c.6137G>A MANE Select | NP_001136272.1:p.Trp2046Ter | |
| NM_001292009.2:c.6137G>A | NP_001278938.1:p.Trp2046Ter |