Linked Data
gnomAD v4:
17-41582888-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41582888C>T , CM000679.2:g.41582888C>T | GRCh38 |
| NC_000017.10:g.39739140C>T , CM000679.1:g.39739140C>T | GRCh37 |
| NC_000017.9:g.36992666C>T | NCBI36 |
| NG_008624.1:g.9008G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.1321+206G>A MANE Select | ENSP00000167586.6:n.1321+206G>A | |
| ENST00000167586.6:c.1321+206G>A | ENSP00000167586.6:n.1321+206G>A | |
| ENST00000441550.2:n.474G>A | ||
| NM_000526.4:c.1321+206G>A | NP_000517.2:n.1321+206G>A | |
| NM_000526.5:c.1321+206G>A MANE Select | NP_000517.3:n.1321+206G>A |