Linked Data
gnomAD v4:
11-5253147-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5253147A>G , CM000673.2:g.5253147A>G | GRCh38 |
| NC_000011.9:g.5274377A>G , CM000673.1:g.5274377A>G | GRCh37 |
| NC_000011.8:g.5230953A>G | NCBI36 |
| NG_000007.3:g.44469T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642908.1:c.315+1145T>C | ENSP00000495346.1:n.315+1145T>C | |
| ENST00000647543.1:c.378+196T>C | ENSP00000496470.1:n.378+196T>C | |
| ENST00000620888.4:c.315+1145T>C | ENSP00000479637.1:n.315+1145T>C |