Linked Data
gnomAD v4:
4-186085783-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085783T>C , CM000666.2:g.186085783T>C | GRCh38 |
| NC_000004.11:g.187006937T>C , CM000666.1:g.187006937T>C | GRCh37 |
| NC_000004.10:g.187243931T>C | NCBI36 |
| NG_007278.1:g.21629T>C , LRG_117:g.21629T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698352.1:c.*3177T>C | ENSP00000513675.1:n.*3177T>C | |
| ENST00000698353.1:n.3500T>C | ||
| ENST00000698354.1:c.*910T>C | ENSP00000513676.1:n.*910T>C | |
| ENST00000296795.8:c.*910T>C MANE Select | ENSP00000296795.3:n.*910T>C | |
| ENST00000296795.7:c.*910T>C | ENSP00000296795.2:n.*910T>C | |
| NM_003265.3:c.*910T>C MANE Select | NP_003256.1:n.*910T>C |