Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186679065C>A , CM000663.2:g.186679065C>A | GRCh38 |
| NC_000001.10:g.186648197C>A , CM000663.1:g.186648197C>A | GRCh37 |
| NC_000001.9:g.184914820C>A | NCBI36 |
| NG_028206.2:g.6363G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000963.4:c.306G>T MANE Select | NP_000954.1:p.Val102= |
| ENST00000367468.10:c.306G>T MANE Select | ENSP00000356438.5:p.Val102= |
| NM_000963.3:c.306G>T | NP_000954.1:p.Val102= |
| ENST00000367468.9:c.306G>T | ENSP00000356438.5:p.Val102= |
| ENST00000490885.6:n.439G>T | |
| ENST00000559627.1:c.306G>T | ENSP00000454130.1:p.Val102= |
| ENST00000559800.1:n.439G>T | |
| ENST00000680451.1:c.306G>T | ENSP00000506242.1:p.Val102= |
| ENST00000681605.1:c.306G>T | ENSP00000504900.1:p.Val102= |