Linked Data
ClinVar Variation Id:
865964
dbSNP Id:
rs1801269
gnomAD v2:
1-94506901-C-T
gnomAD v3:
1-94041345-C-T
gnomAD v4:
1-94041345-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94041345C>T , CM000663.2:g.94041345C>T | GRCh38 |
| NC_000001.10:g.94506901C>T , CM000663.1:g.94506901C>T | GRCh37 |
| NC_000001.9:g.94279489C>T | NCBI36 |
| NG_009073.1:g.84805G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.3386G>A MANE Select | ENSP00000359245.3:p.Arg1129His | |
| ENST00000370225.3:c.3386G>A | ENSP00000359245.3:p.Arg1129His | |
| ENST00000536513.5:c.-64-1256G>A | ENSP00000439707.2:n.-64-1256G>A | |
| NM_000350.2:c.3386G>A | NP_000341.2:p.Arg1129His | |
| NM_000350.3:c.3386G>A MANE Select | NP_000341.2:p.Arg1129His |