Linked Data
gnomAD v4:
10-122508659-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122508659G>C , CM000672.2:g.122508659G>C | GRCh38 |
| NC_000010.10:g.124268175G>C , CM000672.1:g.124268175G>C | GRCh37 |
| NC_000010.9:g.124258165G>C | NCBI36 |
| NG_011554.1:g.52135G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.1009G>C MANE Select | ENSP00000357980.3:p.Gly337Arg | |
| ENST00000648167.1:c.691G>C | ENSP00000498033.1:p.Gly231Arg | |
| ENST00000368984.7:c.1009G>C | ENSP00000357980.3:p.Gly337Arg | |
| ENST00000420892.1:c.232G>C | ENSP00000412676.1:p.Gly78Arg | |
| NM_002775.4:c.1009G>C | NP_002766.1:p.Gly337Arg | |
| NM_002775.5:c.1009G>C MANE Select | NP_002766.1:p.Gly337Arg |