Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67066190G>T , CM000677.2:g.67066190G>T | GRCh38 |
| NC_000015.9:g.67358528G>T , CM000677.1:g.67358528G>T | GRCh37 |
| NC_000015.8:g.65145582G>T | NCBI36 |
| NG_011990.1:g.5334G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559460.6:c.-110+2246G>T | ENSP00000453082.2:n.-110+2246G>T | |
| ENST00000560424.2:c.36G>T | ENSP00000455540.2:p.Val12= | |
| ENST00000327367.9:c.36G>T MANE Select | ENSP00000332973.4:p.Val12= | |
| ENST00000327367.8:c.36G>T | ENSP00000332973.4:p.Val12= | |
| ENST00000559460.5:c.-110+2246G>T | ENSP00000453082.1:n.-110+2246G>T | |
| NM_005902.3:c.36G>T | NP_005893.1:p.Val12= | |
| XM_011521559.1:c.36G>T | XP_011519861.1:p.Val12= | |
| XM_011521559.3:c.36G>T | XP_011519861.1:p.Val12= | |
| NM_005902.4:c.36G>T MANE Select | NP_005893.1:p.Val12= |