Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60648658T>A , CM000676.2:g.60648658T>A | GRCh38 |
| NC_000014.8:g.61115376T>A , CM000676.1:g.61115376T>A | GRCh37 |
| NC_000014.7:g.60185129T>A | NCBI36 |
| NG_008231.1:g.5780A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645694.3:c.532A>T (SIX1) MANE Select | ENSP00000494686.1:p.Arg178Ter | |
| ENST00000247182.6:c.532A>T (SIX1) | ENSP00000247182.5:p.Arg178Ter | |
| ENST00000553535.2:n.249-2081A>T (SIX1) | ||
| ENST00000554986.2:c.42-2081A>T (SIX1) | ENSP00000452700.2:n.42-2081A>T | |
| ENST00000555955.3:n.1198-2081A>T (SIX1) | ||
| NM_005982.3:c.532A>T (SIX1) | NP_005973.1:p.Arg178Ter | |
| XM_017021602.2:c.501+31A>T (SIX1) | XP_016877091.1:n.501+31A>T | |
| NM_005982.4:c.532A>T (SIX1) MANE Select | NP_005973.1:p.Arg178Ter | |
| NR_162089.1:n.11T>A (MIR9718) |