Linked Data
ClinVar Variation Id:
2850412
ClinVar RCV Id:
RCV003763276
dbSNP Id:
rs1441528201
gnomAD v2:
1-169524407-C-T
gnomAD v4:
1-169555169-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169555169C>T , CM000663.2:g.169555169C>T | GRCh38 |
| NC_000001.10:g.169524407C>T , CM000663.1:g.169524407C>T | GRCh37 |
| NC_000001.9:g.167791031C>T | NCBI36 |
| NG_011806.1:g.36363G>A , LRG_553:g.36363G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1118+13G>A MANE Select | ENSP00000356771.3:n.1118+13G>A | |
| ENST00000367796.3:c.1118+13G>A | ENSP00000356770.3:n.1118+13G>A | |
| ENST00000367797.7:c.1118+13G>A | ENSP00000356771.3:n.1118+13G>A | |
| NM_000130.4:c.1118+13G>A , LRG_553t1:c.1118+13G>A | NP_000121.2:n.1118+13G>A | |
| XM_017000660.2:c.707+13G>A | XP_016856149.1:n.707+13G>A | |
| NM_000130.5:c.1118+13G>A MANE Select | NP_000121.2:n.1118+13G>A |