Linked Data
gnomAD v4:
10-122461713-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461713T>C , CM000672.2:g.122461713T>C | GRCh38 |
| NC_000010.10:g.124221229T>C , CM000672.1:g.124221229T>C | GRCh37 |
| NC_000010.9:g.124211219T>C | NCBI36 |
| NG_011554.1:g.5189T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.61T>C MANE Select | ENSP00000357980.3:p.Ser21Pro | |
| ENST00000648167.1:c.154+3004T>C | ENSP00000498033.1:n.154+3004T>C | |
| ENST00000368984.7:c.61T>C | ENSP00000357980.3:p.Ser21Pro | |
| NM_002775.4:c.61T>C | NP_002766.1:p.Ser21Pro | |
| NM_002775.5:c.61T>C MANE Select | NP_002766.1:p.Ser21Pro |