Linked Data
dbSNP Id:
rs757421299
ExAC:
1:94506778 C / T
gnomAD v2:
1-94506778-C-T
COSMIC:
COSM3493473
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94041222C>T , CM000663.2:g.94041222C>T | GRCh38 |
| NC_000001.10:g.94506778C>T , CM000663.1:g.94506778C>T | GRCh37 |
| NC_000001.9:g.94279366C>T | NCBI36 |
| NG_009073.1:g.84928G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.3509G>A MANE Select | ENSP00000359245.3:p.Arg1170Lys | |
| ENST00000370225.3:c.3509G>A | ENSP00000359245.3:p.Arg1170Lys | |
| ENST00000536513.5:c.-64-1133G>A | ENSP00000439707.2:n.-64-1133G>A | |
| NM_000350.2:c.3509G>A | NP_000341.2:p.Arg1170Lys | |
| NM_000350.3:c.3509G>A MANE Select | NP_000341.2:p.Arg1170Lys |