Linked Data
gnomAD v4:
17-42544213-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42544213C>G , CM000679.2:g.42544213C>G | GRCh38 |
| NC_000017.10:g.40696231C>G , CM000679.1:g.40696231C>G | GRCh37 |
| NC_000017.9:g.37949757C>G | NCBI36 |
| NG_011552.1:g.13281C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.2207C>G MANE Select | ENSP00000225927.1:p.Pro736Arg | |
| ENST00000225927.6:c.2207C>G | ENSP00000225927.1:p.Pro736Arg | |
| NM_000263.3:c.2207C>G | NP_000254.2:p.Pro736Arg | |
| XM_006721920.2:c.1376C>G | XP_006721983.1:p.Pro459Arg | |
| XM_011524840.1:c.1208C>G | XP_011523142.1:p.Pro403Arg | |
| XM_017024687.1:c.1376C>G | XP_016880176.1:p.Pro459Arg | |
| XM_024450771.1:c.2264C>G | XP_024306539.1:p.Pro755Arg | |
| XM_024450772.1:c.1208C>G | XP_024306540.1:p.Pro403Arg | |
| NM_000263.4:c.2207C>G MANE Select | NP_000254.2:p.Pro736Arg |