Linked Data
ClinVar Variation Id:
1540746
ClinVar RCV Id:
RCV002157246
dbSNP Id:
rs756865172
ExAC:
4:106967844 A / G
gnomAD v2:
4-106967844-A-G
gnomAD v3:
4-106046687-A-G
gnomAD v4:
4-106046687-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.106046687A>G , CM000666.2:g.106046687A>G | GRCh38 |
| NC_000004.11:g.106967844A>G , CM000666.1:g.106967844A>G | GRCh37 |
| NC_000004.10:g.107187293A>G | NCBI36 |
| NG_034057.2:g.279809T>C | |
| NG_034057.3:g.274997T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000273980.10:c.2572-7T>C | ENSP00000273980.4:n.2572-7T>C | |
| ENST00000394708.7:c.2572-7T>C MANE Select | ENSP00000378198.2:n.2572-7T>C | |
| ENST00000273980.9:c.2572-7T>C | ENSP00000273980.4:n.2572-7T>C | |
| ENST00000361687.8:c.2383-7T>C | ENSP00000355338.4:n.2383-7T>C | |
| ENST00000394706.7:c.2455-7T>C | ENSP00000378196.3:n.2455-7T>C | |
| ENST00000394708.6:c.2572-7T>C | ENSP00000378198.2:n.2572-7T>C | |
| ENST00000432496.6:c.2572-7T>C | ENSP00000405847.2:n.2572-7T>C | |
| ENST00000467183.6:c.*2211-7T>C | ENSP00000421182.1:n.*2211-7T>C | |
| ENST00000510927.5:n.2225-7T>C | ||
| NM_001163435.2:c.2572-7T>C | NP_001156907.1:n.2572-7T>C | |
| NM_001163436.2:c.2572-7T>C | NP_001156908.1:n.2572-7T>C | |
| NM_001163437.2:c.2455-7T>C | NP_001156909.1:n.2455-7T>C | |
| NM_001290768.1:c.2056-7T>C | NP_001277697.1:n.2056-7T>C | |
| NM_033115.4:c.2383-7T>C | NP_149106.2:n.2383-7T>C | |
| XM_011532417.1:c.2572-7T>C | XP_011530719.1:n.2572-7T>C | |
| XM_011532418.1:c.2254-7T>C | XP_011530720.1:n.2254-7T>C | |
| XM_011532419.1:c.2056-7T>C | XP_011530721.1:n.2056-7T>C | |
| XM_011532417.2:c.2572-7T>C | XP_011530719.1:n.2572-7T>C | |
| XM_017008846.1:c.2572-7T>C | XP_016864335.1:n.2572-7T>C | |
| XM_017008848.1:c.2254-7T>C | XP_016864337.1:n.2254-7T>C | |
| XM_017008849.1:c.2056-7T>C | XP_016864338.1:n.2056-7T>C | |
| XM_024454281.1:c.2572-7T>C | XP_024310049.1:n.2572-7T>C | |
| XM_024454282.1:c.2572-7T>C | XP_024310050.1:n.2572-7T>C | |
| XR_002959772.1:n.2766-7T>C | ||
| NM_001163435.3:c.2572-7T>C MANE Select | NP_001156907.2:n.2572-7T>C | |
| NM_001163436.4:c.2572-7T>C | NP_001156908.2:n.2572-7T>C | |
| NM_001163437.3:c.2455-7T>C | NP_001156909.2:n.2455-7T>C | |
| NM_001290768.2:c.2056-7T>C | NP_001277697.2:n.2056-7T>C | |
| NM_033115.5:c.2383-7T>C | NP_149106.3:n.2383-7T>C |