Linked Data
gnomAD v4:
17-56594660-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594660A>G , CM000679.2:g.56594660A>G | GRCh38 |
| NC_000017.10:g.54672021A>G , CM000679.1:g.54672021A>G | GRCh37 |
| NC_000017.9:g.52027020A>G | NCBI36 |
| NG_011958.1:g.5962A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332822.6:c.437A>G MANE Select | ENSP00000328181.4:p.Gln146Arg | |
| ENST00000332822.4:c.437A>G | ENSP00000328181.4:p.Gln146Arg | |
| NM_005450.4:c.437A>G | NP_005441.1:p.Gln146Arg | |
| NM_005450.6:c.437A>G MANE Select | NP_005441.1:p.Gln146Arg |