Linked Data
gnomAD v4:
1-1013987-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1013987T>C , CM000663.2:g.1013987T>C | GRCh38 |
| NC_000001.10:g.949367T>C , CM000663.1:g.949367T>C | GRCh37 |
| NC_000001.9:g.939230T>C | NCBI36 |
| NG_033033.1:g.5521T>C | |
| NG_033033.2:g.17850T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624697.4:c.-18T>C | ENSP00000485643.1:n.-18T>C | |
| ENST00000649529.1:c.7T>C MANE Select | ENSP00000496832.1:p.Trp3Arg | |
| ENST00000379389.4:c.7T>C | ENSP00000368699.4:p.Trp3Arg | |
| ENST00000624652.1:c.-18T>C | ENSP00000485313.1:n.-18T>C | |
| ENST00000624697.3:c.-18T>C | ENSP00000485643.1:n.-18T>C | |
| NM_005101.3:c.7T>C | NP_005092.1:p.Trp3Arg | |
| NM_005101.4:c.7T>C MANE Select | NP_005092.1:p.Trp3Arg |