Linked Data
ClinVar Variation Id:
456400
ClinVar RCV Id:
RCV000527551
dbSNP Id:
rs1555602832
gnomAD v4:
17-80117599-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80117599G>C , CM000679.2:g.80117599G>C | GRCh38 |
| NC_000017.10:g.78091398G>C , CM000679.1:g.78091398G>C | GRCh37 |
| NC_000017.9:g.75705993G>C | NCBI36 |
| NG_009822.1:g.21044G>C , LRG_673:g.21044G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.2332-1G>C | ENSP00000460543.2:n.2332-1G>C | |
| ENST00000572080.2:c.*470-1G>C | ENSP00000459972.2:n.*470-1G>C | |
| ENST00000577106.6:c.2332-1G>C | ENSP00000458306.2:n.2332-1G>C | |
| ENST00000302262.8:c.2332-1G>C MANE Select | ENSP00000305692.3:n.2332-1G>C | |
| ENST00000302262.7:c.2332-1G>C | ENSP00000305692.3:n.2332-1G>C | |
| ENST00000390015.7:c.2332-1G>C | ENSP00000374665.3:n.2332-1G>C | |
| ENST00000573556.1:n.285-1G>C | ||
| NM_000152.3:c.2332-1G>C , LRG_673t1:c.2332-1G>C | NP_000143.2:n.2332-1G>C | |
| NM_001079803.1:c.2332-1G>C | NP_001073271.1:n.2332-1G>C | |
| NM_001079804.1:c.2332-1G>C | NP_001073272.1:n.2332-1G>C | |
| XM_005257193.1:c.2332-1G>C | XP_005257250.1:n.2332-1G>C | |
| XM_005257194.3:c.2332-1G>C | XP_005257251.1:n.2332-1G>C | |
| NM_000152.4:c.2332-1G>C | NP_000143.2:n.2332-1G>C | |
| NM_001079803.2:c.2332-1G>C | NP_001073271.1:n.2332-1G>C | |
| NM_001079804.2:c.2332-1G>C | NP_001073272.1:n.2332-1G>C | |
| XM_005257193.2:c.2332-1G>C | XP_005257250.1:n.2332-1G>C | |
| XM_005257194.4:c.2332-1G>C | XP_005257251.1:n.2332-1G>C | |
| NM_000152.5:c.2332-1G>C MANE Select | NP_000143.2:n.2332-1G>C | |
| NM_001079803.3:c.2332-1G>C | NP_001073271.1:n.2332-1G>C | |
| NM_001079804.3:c.2332-1G>C | NP_001073272.1:n.2332-1G>C |