Linked Data
gnomAD v4:
14-50937788-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50937788T>C , CM000676.2:g.50937788T>C | GRCh38 |
| NC_000014.8:g.51404506T>C , CM000676.1:g.51404506T>C | GRCh37 |
| NC_000014.7:g.50474256T>C | NCBI36 |
| NG_012796.1:g.11743A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.293A>G MANE Select | ENSP00000216392.7:p.Asn98Ser | |
| ENST00000216392.7:c.293A>G | ENSP00000216392.7:p.Asn98Ser | |
| ENST00000530336.2:n.360A>G | ||
| ENST00000532462.5:c.293A>G | ENSP00000431657.1:p.Asn98Ser | |
| ENST00000544180.6:c.244-2603A>G | ENSP00000443787.1:n.244-2603A>G | |
| NM_001163940.1:c.244-2603A>G | NP_001157412.1:n.244-2603A>G | |
| NM_002863.4:c.293A>G | NP_002854.3:p.Asn98Ser | |
| NM_002863.5:c.293A>G MANE Select | NP_002854.3:p.Asn98Ser | |
| NM_001163940.2:c.244-2603A>G | NP_001157412.1:n.244-2603A>G |