HGVS | Genome Assembly |
---|---|
NC_000011.10:g.16735399A>G , CM000673.2:g.16735399A>G | GRCh38 |
NC_000011.9:g.16756946A>G , CM000673.1:g.16756946A>G | GRCh37 |
NC_000011.8:g.16713522A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524520.5:n.353+940T>C (SOX6) | ||
ENST00000525259.1:n.267+940T>C (SOX6) | ||
ENST00000527893.5:n.405-9202A>G (C11orf58) | ||
ENST00000530378.5:c.-335+940T>C (SOX6) | ENSP00000432577.1:n.-335+940T>C | |
NM_001367872.1:c.-261+3026T>C (SOX6) | NP_001354801.1:n.-261+3026T>C |