Linked Data
dbSNP Id:
rs1590069543
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.16735367A>G , CM000673.2:g.16735367A>G | GRCh38 |
| NC_000011.9:g.16756914A>G , CM000673.1:g.16756914A>G | GRCh37 |
| NC_000011.8:g.16713490A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524520.5:n.353+972T>C (SOX6) | ||
| ENST00000525259.1:n.267+972T>C (SOX6) | ||
| ENST00000527893.5:n.405-9234A>G (C11orf58) | ||
| ENST00000530378.5:c.-335+972T>C (SOX6) | ENSP00000432577.1:n.-335+972T>C | |
| NM_001367872.1:c.-261+3058T>C (SOX6) | NP_001354801.1:n.-261+3058T>C |