Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23375650C>T , CM000676.2:g.23375650C>T | GRCh38 |
| NC_000014.8:g.23844859C>T , CM000676.1:g.23844859C>T | GRCh37 |
| NC_000014.7:g.22914699C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397242.3:c.256C>T MANE Select | ENSP00000380417.2:p.Pro86Ser | |
| ENST00000329715.2:c.304C>T | ENSP00000328111.2:p.Pro102Ser | |
| ENST00000397242.2:c.256C>T | ENSP00000380417.2:p.Pro86Ser | |
| NM_022789.3:c.304C>T | NP_073626.1:p.Pro102Ser | |
| NM_172314.1:c.256C>T | NP_758525.1:p.Pro86Ser |