Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23375662T>C , CM000676.2:g.23375662T>C | GRCh38 |
| NC_000014.8:g.23844871T>C , CM000676.1:g.23844871T>C | GRCh37 |
| NC_000014.7:g.22914711T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397242.3:c.268T>C MANE Select | ENSP00000380417.2:p.Tyr90His | |
| ENST00000329715.2:c.316T>C | ENSP00000328111.2:p.Tyr106His | |
| ENST00000397242.2:c.268T>C | ENSP00000380417.2:p.Tyr90His | |
| NM_022789.3:c.316T>C | NP_073626.1:p.Tyr106His | |
| NM_172314.1:c.268T>C | NP_758525.1:p.Tyr90His |