Linked Data
gnomAD v4:
17-8075526-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075526A>G , CM000679.2:g.8075526A>G | GRCh38 |
| NC_000017.10:g.7978844A>G , CM000679.1:g.7978844A>G | GRCh37 |
| NC_000017.9:g.7919569A>G | NCBI36 |
| NG_007099.1:g.17178T>C | |
| NG_007099.2:g.17191T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1654+69T>C MANE Select | ENSP00000497784.1:n.1654+69T>C | |
| ENST00000649809.1:c.718+69T>C | ENSP00000496845.1:n.718+69T>C | |
| ENST00000319144.4:c.1654+69T>C | ENSP00000315167.4:n.1654+69T>C | |
| ENST00000577351.5:n.479+649T>C | ||
| NM_001139.2:c.1654+69T>C | NP_001130.1:n.1654+69T>C | |
| NM_001139.3:c.1654+69T>C MANE Select | NP_001130.1:n.1654+69T>C |