Linked Data
dbSNP Id:
rs568839929
ExAC:
15:75042216 G / A
gnomAD v2:
15-75042216-G-A
gnomAD v3:
15-74749875-G-A
gnomAD v4:
15-74749875-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749875G>A , CM000677.2:g.74749875G>A | GRCh38 |
| NC_000015.9:g.75042216G>A , CM000677.1:g.75042216G>A | GRCh37 |
| NC_000015.8:g.72829269G>A | NCBI36 |
| NG_008431.1:g.32334G>A | |
| NG_008431.2:g.32334G>A | |
| NG_061543.1:g.6031G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.137G>A MANE Select | ENSP00000342007.4:p.Trp46Ter | |
| ENST00000343932.4:c.137G>A | ENSP00000342007.4:p.Trp46Ter | |
| NM_000761.4:c.137G>A | NP_000752.2:p.Trp46Ter | |
| NM_000761.5:c.137G>A MANE Select | NP_000752.2:p.Trp46Ter |