Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173531T>C , CM000678.2:g.173531T>C | GRCh38 |
| NC_000016.9:g.223530T>C , CM000678.1:g.223530T>C | GRCh37 |
| NC_000016.8:g.163530T>C | NCBI36 |
| NG_000006.1:g.34394T>C | |
| NG_059186.1:g.1881T>C | |
| NG_059271.1:g.5685T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.360T>C MANE Select | ENSP00000251595.6:p.Pro120= | |
| ENST00000251595.10:c.360T>C | ENSP00000251595.6:p.Pro120= | |
| ENST00000397806.1:c.264T>C | ENSP00000380908.1:p.Pro88= | |
| ENST00000482565.1:n.496T>C | ||
| NM_000517.4:c.360T>C | NP_000508.1:p.Pro120= | |
| NM_000517.6:c.360T>C MANE Select | NP_000508.1:p.Pro120= |