Linked Data
ClinVar Variation Id:
2836564
ClinVar RCV Id:
RCV003648393
dbSNP Id:
rs1251991373
gnomAD v2:
7-150654368-T-C
gnomAD v4:
7-150957280-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150957280T>C , CM000669.2:g.150957280T>C | GRCh38 |
| NC_000007.13:g.150654368T>C , CM000669.1:g.150654368T>C | GRCh37 |
| NC_000007.12:g.150285301T>C | NCBI36 |
| NG_008916.1:g.25647A>G , LRG_288:g.25647A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.1961+11A>G | ||
| ENST00000262186.10:c.1128+11A>G MANE Select | ENSP00000262186.5:n.1128+11A>G | |
| ENST00000262186.9:c.1128+11A>G | ENSP00000262186.5:n.1128+11A>G | |
| ENST00000430723.4:c.780+11A>G | ENSP00000387657.4:n.780+11A>G | |
| ENST00000532957.5:n.1351+11A>G | ||
| NM_000238.3:c.1128+11A>G , LRG_288t1:c.1128+11A>G | NP_000229.1:n.1128+11A>G | |
| NM_172056.2:c.1128+11A>G , LRG_288t2:c.1128+11A>G | NP_742053.1:n.1128+11A>G | |
| XM_011516185.1:c.828+11A>G | XP_011514487.1:n.828+11A>G | |
| XM_011516186.1:c.1128+11A>G | XP_011514488.1:n.1128+11A>G | |
| XM_011516185.2:c.828+11A>G | XP_011514487.1:n.828+11A>G | |
| XM_011516186.3:c.1128+11A>G | XP_011514488.1:n.1128+11A>G | |
| XM_017012195.1:c.978+11A>G | XP_016867684.1:n.978+11A>G | |
| XM_017012196.1:c.951+11A>G | XP_016867685.1:n.951+11A>G | |
| NM_000238.4:c.1128+11A>G MANE Select | NP_000229.1:n.1128+11A>G |