HGVS | Genome Assembly |
---|---|
NC_000010.11:g.14436622A>T , CM000672.2:g.14436622A>T | GRCh38 |
NC_000010.10:g.14478621A>T , CM000672.1:g.14478621A>T | GRCh37 |
NC_000010.9:g.14518627A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000475141.2:c.-305+25446T>A (FRMD4A) | ENSP00000473870.1:n.-305+25446T>A | |
ENST00000493380.5:c.-82+25446T>A (FRMD4A) | ENSP00000474863.1:n.-82+25446T>A | |
NR_031668.1:n.47A>T (MIR1265) |