Linked Data
dbSNP Id:
rs1729843385
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99149863C>G , CM000666.2:g.99149863C>G | GRCh38 |
| NC_000004.11:g.100071020C>G , CM000666.1:g.100071020C>G | GRCh37 |
| NC_000004.10:g.100290043C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504581.1:n.170-7083G>C | ||
| NR_037884.1:n.680-4682C>G |