Linked Data
MyVariant Identifiers:
chr10:g.14478619T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.14436620T>C , CM000672.2:g.14436620T>C | GRCh38 |
| NC_000010.10:g.14478619T>C , CM000672.1:g.14478619T>C | GRCh37 |
| NC_000010.9:g.14518625T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000475141.2:c.-305+25448A>G (FRMD4A) | ENSP00000473870.1:n.-305+25448A>G | |
| ENST00000493380.5:c.-82+25448A>G (FRMD4A) | ENSP00000474863.1:n.-82+25448A>G | |
| NR_031668.1:n.45T>C (MIR1265) |