HGVS | Genome Assembly |
---|---|
NC_000011.10:g.16735532C>T , CM000673.2:g.16735532C>T | GRCh38 |
NC_000011.9:g.16757079C>T , CM000673.1:g.16757079C>T | GRCh37 |
NC_000011.8:g.16713655C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524520.5:n.353+807G>A (SOX6) | ||
ENST00000525259.1:n.267+807G>A (SOX6) | ||
ENST00000527893.5:n.405-9069C>T (C11orf58) | ||
ENST00000530378.5:c.-335+807G>A (SOX6) | ENSP00000432577.1:n.-335+807G>A | |
NM_001367872.1:c.-261+2893G>A (SOX6) | NP_001354801.1:n.-261+2893G>A |