Linked Data
ClinVar Variation Id:
177959
ClinVar RCV Id:
RCV000154623
RCV000157861
RCV000220945
RCV000705134
RCV000722039
RCV001678585
RCV001808423
dbSNP Id:
rs727504426
COSMIC:
COSM34065
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119278508A>G , CM000673.2:g.119278508A>G | GRCh38 |
| NC_000011.9:g.119149218A>G , CM000673.1:g.119149218A>G | GRCh37 |
| NC_000011.8:g.118654428A>G | NCBI36 |
| NG_016808.1:g.77229A>G , LRG_608:g.77229A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700472.1:c.*680-2A>G | ENSP00000515005.1:n.*680-2A>G | |
| ENST00000264033.6:c.1228-2A>G MANE Select | ENSP00000264033.3:n.1228-2A>G | |
| ENST00000637974.1:c.1222-2A>G | ENSP00000490763.1:n.1222-2A>G | |
| ENST00000264033.5:c.1228-2A>G | ENSP00000264033.3:n.1228-2A>G | |
| ENST00000634586.1:c.1228-2A>G | ENSP00000489218.1:n.1228-2A>G | |
| ENST00000634840.1:c.1228-2A>G | ENSP00000489324.1:n.1228-2A>G | |
| NM_005188.3:c.1228-2A>G , LRG_608t1:c.1228-2A>G | NP_005179.2:n.1228-2A>G | |
| XM_011543057.1:c.1228-2A>G | XP_011541359.1:n.1228-2A>G | |
| NM_005188.4:c.1228-2A>G MANE Select | NP_005179.2:n.1228-2A>G |