Linked Data
ClinVar Variation Id:
859013
ClinVar RCV Id:
RCV001065022
dbSNP Id:
rs770565005
ExAC:
1:94526309 C / A
gnomAD v2:
1-94526309-C-A
gnomAD v3:
1-94060753-C-A
gnomAD v4:
1-94060753-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94060753C>A , CM000663.2:g.94060753C>A | GRCh38 |
| NC_000001.10:g.94526309C>A , CM000663.1:g.94526309C>A | GRCh37 |
| NC_000001.9:g.94298897C>A | NCBI36 |
| NG_009073.1:g.65397G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.1944G>T MANE Select | ENSP00000359245.3:p.Met648Ile | |
| ENST00000649773.1:c.1944G>T | ENSP00000496882.1:p.Met648Ile | |
| ENST00000370225.3:c.1944G>T | ENSP00000359245.3:p.Met648Ile | |
| ENST00000472033.1:n.64G>T | ||
| ENST00000536513.5:c.-65+2421G>T | ENSP00000439707.2:n.-65+2421G>T | |
| NM_000350.2:c.1944G>T | NP_000341.2:p.Met648Ile | |
| NM_000350.3:c.1944G>T MANE Select | NP_000341.2:p.Met648Ile |