Linked Data
ClinVar Variation Id:
180949
ClinVar RCV Id:
RCV000158116
dbSNP Id:
rs112179534
gnomAD v4:
11-47341246-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47341246T>G , CM000673.2:g.47341246T>G | GRCh38 |
| NC_000011.9:g.47362797T>G , CM000673.1:g.47362797T>G | GRCh37 |
| NC_000011.8:g.47319373T>G | NCBI36 |
| NG_007667.1:g.16457A>C , LRG_386:g.16457A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000545968.6:c.1791-2A>C MANE Select | ENSP00000442795.1:n.1791-2A>C | |
| ENST00000256993.8:c.1791-2A>C | ENSP00000256993.5:n.1791-2A>C | |
| ENST00000399249.6:c.1791-2A>C | ENSP00000382193.2:n.1791-2A>C | |
| ENST00000544791.1:c.1791-2A>C | ENSP00000444259.1:n.1791-2A>C | |
| ENST00000545968.5:c.1791-2A>C | ENSP00000442795.1:n.1791-2A>C | |
| NM_000256.3:c.1791-2A>C , LRG_386t1:c.1791-2A>C MANE Select | NP_000247.2:n.1791-2A>C | |
| XM_011520117.1:c.1773-2A>C | XP_011518419.1:n.1773-2A>C | |
| XM_011520118.1:c.1791-2A>C | XP_011518420.1:n.1791-2A>C |