Linked Data
ClinVar Variation Id:
457217
ClinVar RCV Id:
RCV000551908
dbSNP Id:
rs1555397195
COSMIC:
COSM6049352
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48468411C>A , CM000677.2:g.48468411C>A | GRCh38 |
| NC_000015.9:g.48760608C>A , CM000677.1:g.48760608C>A | GRCh37 |
| NC_000015.8:g.46547900C>A | NCBI36 |
| NG_008805.2:g.182378G>T , LRG_778:g.182378G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4582+1G>T | ENSP00000453958.2:n.4582+1G>T | |
| ENST00000674301.2:c.4582+1G>T | ENSP00000501333.2:n.4582+1G>T | |
| ENST00000684448.1:n.3256+1G>T | ||
| ENST00000316623.10:c.4582+1G>T MANE Select | ENSP00000325527.5:n.4582+1G>T | |
| ENST00000316623.9:c.4582+1G>T | ENSP00000325527.5:n.4582+1G>T | |
| ENST00000537463.6:c.*345+1G>T | ENSP00000440294.2:n.*345+1G>T | |
| NM_000138.4:c.4582+1G>T , LRG_778t1:c.4582+1G>T | NP_000129.3:n.4582+1G>T | |
| NM_000138.5:c.4582+1G>T MANE Select | NP_000129.3:n.4582+1G>T |