Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177376T>C , CM000678.2:g.177376T>C | GRCh38 |
| NC_000016.9:g.227375T>C , CM000678.1:g.227375T>C | GRCh37 |
| NC_000016.8:g.167375T>C | NCBI36 |
| NG_000006.1:g.38239T>C | |
| NG_059186.1:g.5726T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.394T>C MANE Select | ENSP00000322421.5:p.Ser132Pro | |
| ENST00000397797.1:c.298T>C | ENSP00000380899.1:p.Ser100Pro | |
| ENST00000472694.1:n.530T>C | ||
| NM_000558.4:c.394T>C | NP_000549.1:p.Ser132Pro | |
| NM_000558.5:c.394T>C MANE Select | NP_000549.1:p.Ser132Pro |