Linked Data
ClinVar Variation Id:
102903
dbSNP Id:
rs62642914
gnomAD v4:
12-102846926-G-A
ERepo:
CA229861/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102846926G>A , CM000674.2:g.102846926G>A | GRCh38 |
| NC_000012.11:g.103240704G>A , CM000674.1:g.103240704G>A | GRCh37 |
| NC_000012.10:g.101764834G>A | NCBI36 |
| NG_008690.1:g.75677C>T | |
| NG_008690.2:g.116485C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.938C>T MANE Select | ENSP00000448059.1:p.Ala313Val | |
| ENST00000307000.7:c.923C>T | ENSP00000303500.2:p.Ala308Val | |
| ENST00000549247.6:n.697C>T | ||
| ENST00000551114.2:n.600C>T | ||
| ENST00000553106.5:c.938C>T | ENSP00000448059.1:p.Ala313Val | |
| ENST00000635477.1:c.74-2495C>T | ||
| ENST00000635528.1:n.453C>T | ||
| NM_000277.1:c.938C>T | NP_000268.1:p.Ala313Val | |
| XM_011538422.1:c.913-2495C>T | XP_011536724.1:n.913-2495C>T | |
| NM_000277.2:c.938C>T | NP_000268.1:p.Ala313Val | |
| NM_001354304.1:c.938C>T | NP_001341233.1:p.Ala313Val | |
| NM_000277.3:c.938C>T MANE Select | NP_000268.1:p.Ala313Val | |
| NM_001354304.2:c.938C>T | NP_001341233.1:p.Ala313Val |