Linked Data
dbSNP Id:
rs2090137793
gnomAD v4:
20-49905811-A-G
MyVariant Identifiers:
chr20:g.48522348A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.49905811A>G , CM000682.2:g.49905811A>G | GRCh38 |
| NC_000020.10:g.48522348A>G , CM000682.1:g.48522348A>G | GRCh37 |
| NC_000020.9:g.47955755A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289431.10:c.1371T>C MANE Select | ENSP00000289431.5:p.Thr457= | |
| ENST00000289431.9:c.1371T>C | ENSP00000289431.5:p.Thr457= | |
| ENST00000422556.1:c.1371T>C | ENSP00000416799.1:p.Thr457= | |
| NM_001135773.1:c.1371T>C | NP_001129245.1:p.Thr457= | |
| NM_006038.3:c.1371T>C | NP_006029.1:p.Thr457= | |
| XM_006723894.1:c.1371T>C | XP_006723957.1:p.Thr457= | |
| XM_011529116.1:c.1371T>C | XP_011527418.1:p.Thr457= | |
| NM_006038.4:c.1371T>C MANE Select | NP_006029.1:p.Thr457= | |
| NM_001135773.2:c.1371T>C | NP_001129245.1:p.Thr457= |