Linked Data
gnomAD v4:
11-17642217-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17642217C>G , CM000673.2:g.17642217C>G | GRCh38 |
| NC_000011.9:g.17663764C>G , CM000673.1:g.17663764C>G | GRCh37 |
| NC_000011.8:g.17620340C>G | NCBI36 |
| NG_033191.1:g.99845C>G | |
| NG_033191.2:g.99845C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.8422C>G | ENSP00000382323.2:p.Pro2808Ala | |
| ENST00000399397.6:c.8386C>G MANE Select | ENSP00000382329.2:p.Pro2796Ala | |
| ENST00000399391.6:c.8422C>G | ENSP00000382323.2:p.Pro2808Ala | |
| ENST00000399397.5:c.8386C>G | ENSP00000382329.2:p.Pro2796Ala | |
| NM_001277269.1:c.8422C>G | NP_001264198.1:p.Pro2808Ala | |
| NM_001292063.1:c.8386C>G | NP_001278992.1:p.Pro2796Ala | |
| NM_001277269.2:c.8422C>G | NP_001264198.1:p.Pro2808Ala | |
| NM_001292063.2:c.8386C>G MANE Select | NP_001278992.1:p.Pro2796Ala |