Linked Data
ClinVar Variation Id:
2322338
ClinVar RCV Id:
RCV004164714
dbSNP Id:
rs79477244
gnomAD v4:
15-89792502-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89792502C>G , CM000677.2:g.89792502C>G | GRCh38 |
| NC_000015.9:g.90335733C>G , CM000677.1:g.90335733C>G | GRCh37 |
| NC_000015.8:g.88136737C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300060.7:c.2310G>C MANE Select | ENSP00000300060.6:p.Glu770Asp | |
| ENST00000559874.2:c.2310G>C | ENSP00000452934.2:p.Glu770Asp | |
| ENST00000560137.2:c.2310G>C | ENSP00000453413.2:p.Glu770Asp | |
| ENST00000679248.1:c.2310G>C | ENSP00000502886.1:p.Glu770Asp | |
| ENST00000300060.6:c.2310G>C | ENSP00000300060.6:p.Glu770Asp | |
| ENST00000558740.1:n.214G>C | ||
| NM_001150.2:c.2310G>C | NP_001141.2:p.Glu770Asp | |
| XM_005254892.3:c.2310G>C | XP_005254949.1:p.Glu770Asp | |
| XM_011521473.1:c.2310G>C | XP_011519775.1:p.Glu770Asp | |
| XM_005254892.4:c.2310G>C | XP_005254949.1:p.Glu770Asp | |
| NM_001150.3:c.2310G>C MANE Select | NP_001141.2:p.Glu770Asp | |
| NM_001381923.1:c.2310G>C | NP_001368852.1:p.Glu770Asp | |
| NM_001381924.1:c.2310G>C | NP_001368853.1:p.Glu770Asp |