Linked Data
dbSNP Id:
rs201647779
ExAC:
20:48522394 C / T
gnomAD v2:
20-48522394-C-T
gnomAD v4:
20-49905857-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.49905857C>T , CM000682.2:g.49905857C>T | GRCh38 |
| NC_000020.10:g.48522394C>T , CM000682.1:g.48522394C>T | GRCh37 |
| NC_000020.9:g.47955801C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289431.10:c.1325G>A MANE Select | ENSP00000289431.5:p.Arg442His | |
| ENST00000289431.9:c.1325G>A | ENSP00000289431.5:p.Arg442His | |
| ENST00000422556.1:c.1325G>A | ENSP00000416799.1:p.Arg442His | |
| NM_001135773.1:c.1325G>A | NP_001129245.1:p.Arg442His | |
| NM_006038.3:c.1325G>A | NP_006029.1:p.Arg442His | |
| XM_006723894.1:c.1325G>A | XP_006723957.1:p.Arg442His | |
| XM_011529116.1:c.1325G>A | XP_011527418.1:p.Arg442His | |
| NM_006038.4:c.1325G>A MANE Select | NP_006029.1:p.Arg442His | |
| NM_001135773.2:c.1325G>A | NP_001129245.1:p.Arg442His |