Linked Data
MyVariant Identifiers:
chr19:g.13947283A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13836469A>G , CM000681.2:g.13836469A>G | GRCh38 |
| NC_000019.9:g.13947283A>G , CM000681.1:g.13947283A>G | GRCh37 |
| NC_000019.8:g.13808283A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_029501.1:n.49T>C (MIR27A) | ||
| NR_036515.2:n.6450T>C (MIR23AHG) |