Linked Data
dbSNP Id:
rs1685778495
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149798723G>T , CM000664.2:g.149798723G>T | GRCh38 |
| NC_000002.11:g.150655237G>T , CM000664.1:g.150655237G>T | GRCh37 |
| NC_000002.10:g.150363483G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110240.1:n.536-49186G>T (MMADHC-DT) | ||
| NR_145421.1:n.1341+5459C>A (LINC01931) |