Linked Data
ClinVar Variation Id:
1065378
ClinVar RCV Id:
RCV001375896
dbSNP Id:
rs2136639453
COSMIC:
COSM5023686
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102846891T>A , CM000674.2:g.102846891T>A | GRCh38 |
| NC_000012.11:g.103240669T>A , CM000674.1:g.103240669T>A | GRCh37 |
| NC_000012.10:g.101764799T>A | NCBI36 |
| NG_008690.1:g.75712A>T | |
| NG_008690.2:g.116520A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.969+4A>T MANE Select | ENSP00000448059.1:n.969+4A>T | |
| ENST00000307000.7:c.954+4A>T | ENSP00000303500.2:n.954+4A>T | |
| ENST00000549247.6:n.728+4A>T | ||
| ENST00000551114.2:n.631+4A>T | ||
| ENST00000553106.5:c.969+4A>T | ENSP00000448059.1:n.969+4A>T | |
| ENST00000635477.1:c.74-2460A>T | ||
| ENST00000635528.1:n.484+4A>T | ||
| NM_000277.1:c.969+4A>T | NP_000268.1:n.969+4A>T | |
| XM_011538422.1:c.913-2460A>T | XP_011536724.1:n.913-2460A>T | |
| NM_000277.2:c.969+4A>T | NP_000268.1:n.969+4A>T | |
| NM_001354304.1:c.969+4A>T | NP_001341233.1:n.969+4A>T | |
| NM_000277.3:c.969+4A>T MANE Select | NP_000268.1:n.969+4A>T | |
| NM_001354304.2:c.969+4A>T | NP_001341233.1:n.969+4A>T |