Linked Data
gnomAD v4:
11-121307297-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121307297C>G , CM000673.2:g.121307297C>G | GRCh38 |
| NC_000011.9:g.121178006C>G , CM000673.1:g.121178006C>G | GRCh37 |
| NC_000011.8:g.120683216C>G | NCBI36 |
| NG_009446.1:g.19619C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264027.9:c.685C>G MANE Select | ENSP00000264027.4:p.His229Asp | |
| ENST00000264027.8:c.685C>G | ENSP00000264027.4:p.His229Asp | |
| ENST00000392789.2:c.685C>G | ENSP00000376539.2:p.His229Asp | |
| ENST00000527183.1:n.978C>G | ||
| ENST00000534230.5:c.631+54C>G | ENSP00000432550.1:n.631+54C>G | |
| NM_001024956.2:c.685C>G | NP_001020127.1:p.His229Asp | |
| NM_006918.4:c.685C>G | NP_008849.2:p.His229Asp | |
| NM_006918.5:c.685C>G MANE Select | NP_008849.2:p.His229Asp | |
| NM_001024956.3:c.685C>G | NP_001020127.1:p.His229Asp |