Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985921T>C , CM000678.2:g.1985921T>C | GRCh38 |
| NC_000016.9:g.2035922T>C , CM000678.1:g.2035922T>C | GRCh37 |
| NC_000016.8:g.1975923T>C | NCBI36 |
| NG_016288.1:g.6773T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.286T>C | ENSP00000455885.1:p.Cys96Arg | |
| ENST00000248114.7:c.511T>C MANE Select | ENSP00000248114.6:p.Cys171Arg | |
| ENST00000248114.6:c.511T>C | ENSP00000248114.6:p.Cys171Arg | |
| ENST00000565658.1:n.668T>C | ||
| ENST00000567719.1:c.286T>C | ENSP00000455885.1:p.Cys96Arg | |
| ENST00000569451.1:c.314T>C | ENSP00000456432.1:p.Val105Ala | |
| NM_005262.2:c.511T>C | NP_005253.3:p.Cys171Arg | |
| NM_005262.3:c.511T>C MANE Select | NP_005253.3:p.Cys171Arg |