Linked Data
dbSNP Id:
rs1685778742
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149798737G>A , CM000664.2:g.149798737G>A | GRCh38 |
| NC_000002.11:g.150655251G>A , CM000664.1:g.150655251G>A | GRCh37 |
| NC_000002.10:g.150363497G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110240.1:n.536-49172G>A (MMADHC-DT) | ||
| NR_145421.1:n.1341+5445C>T (LINC01931) |