Linked Data
dbSNP Id:
rs1848383685
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.16735348T>C , CM000673.2:g.16735348T>C | GRCh38 |
| NC_000011.9:g.16756895T>C , CM000673.1:g.16756895T>C | GRCh37 |
| NC_000011.8:g.16713471T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524520.5:n.353+991A>G (SOX6) | ||
| ENST00000525259.1:n.267+991A>G (SOX6) | ||
| ENST00000527893.5:n.405-9253T>C (C11orf58) | ||
| ENST00000530378.5:c.-335+991A>G (SOX6) | ENSP00000432577.1:n.-335+991A>G | |
| NM_001367872.1:c.-261+3077A>G (SOX6) | NP_001354801.1:n.-261+3077A>G |