Linked Data
dbSNP Id:
rs540200781
gnomAD v2:
17-10030966-C-T
gnomAD v3:
17-10127649-C-T
gnomAD v4:
17-10127649-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10127649C>T , CM000679.2:g.10127649C>T | GRCh38 |
| NC_000017.10:g.10030966C>T , CM000679.1:g.10030966C>T | GRCh37 |
| NC_000017.9:g.9971691C>T | NCBI36 |
| NG_029502.1:g.75903G>A | |
| NG_029502.2:g.75903G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432992.7:c.183+70559G>A MANE Select | ENSP00000407552.2:n.183+70559G>A | |
| ENST00000432992.6:c.183+70559G>A | ENSP00000407552.2:n.183+70559G>A | |
| NM_201433.1:c.183+70559G>A | NP_958839.1:n.183+70559G>A | |
| NM_201433.2:c.183+70559G>A MANE Select | NP_958839.1:n.183+70559G>A |