Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60509891A= , CM000676.2:g.60509891A= | GRCh38 |
| NC_000014.8:g.60976609A= , CM000676.1:g.60976609A= | GRCh37 |
| NC_000014.7:g.60046362A= | NCBI36 |
| NG_008203.1:g.5672A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007374.3:c.493A= (SIX6) MANE Select | NP_031400.2:p.Thr165= |
| ENST00000327720.6:c.493A= (SIX6) MANE Select | ENSP00000328596.5:p.Thr165= |
| NM_007374.2:c.493A= (SIX6) | NP_031400.2:p.Thr165= |
| ENST00000327720.5:c.493A= (SIX6) | ENSP00000328596.5:p.Thr165= |
| ENST00000556799.1:c.-144+5504T= (C14orf39) | ENSP00000451441.1:n.-144+5504T= |