Linked Data
gnomAD v4:
20-10673434-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673434G>T , CM000682.2:g.10673434G>T | GRCh38 |
| NC_000020.10:g.10654082G>T , CM000682.1:g.10654082G>T | GRCh37 |
| NC_000020.9:g.10602082G>T | NCBI36 |
| NG_007496.1:g.5613C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.81+16C>A MANE Select | ENSP00000254958.4:n.81+16C>A | |
| ENST00000254958.9:c.81+16C>A | ENSP00000254958.4:n.81+16C>A | |
| NM_000214.2:c.81+16C>A | NP_000205.1:n.81+16C>A | |
| NM_000214.3:c.81+16C>A MANE Select | NP_000205.1:n.81+16C>A |