Linked Data
gnomAD v4:
5-173232649-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232649C>G , CM000667.2:g.173232649C>G | GRCh38 |
| NC_000005.9:g.172659652C>G , CM000667.1:g.172659652C>G | GRCh37 |
| NC_000005.8:g.172592258C>G | NCBI36 |
| NG_013340.1:g.7664G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.895G>C MANE Select | ENSP00000327758.4:p.Asp299His | |
| ENST00000329198.4:c.895G>C | ENSP00000327758.4:p.Asp299His | |
| NM_001166175.1:c.*848G>C | NP_001159647.1:n.*848G>C | |
| NM_001166176.1:c.*694G>C | NP_001159648.1:n.*694G>C | |
| NM_004387.3:c.895G>C | NP_004378.1:p.Asp299His | |
| NM_004387.4:c.895G>C MANE Select | NP_004378.1:p.Asp299His | |
| NM_001166175.2:c.*848G>C | NP_001159647.1:n.*848G>C | |
| NM_001166176.2:c.*694G>C | NP_001159648.1:n.*694G>C |