Linked Data
MyVariant Identifiers:
chr10:g.14478629T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.14436630T>A , CM000672.2:g.14436630T>A | GRCh38 |
| NC_000010.10:g.14478629T>A , CM000672.1:g.14478629T>A | GRCh37 |
| NC_000010.9:g.14518635T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000475141.2:c.-305+25438A>T (FRMD4A) | ENSP00000473870.1:n.-305+25438A>T | |
| ENST00000493380.5:c.-82+25438A>T (FRMD4A) | ENSP00000474863.1:n.-82+25438A>T | |
| NR_031668.1:n.55T>A (MIR1265) |