Linked Data
dbSNP Id:
rs1799485166
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.122626925G>C , CM000666.2:g.122626925G>C | GRCh38 |
| NC_000004.11:g.123548080G>C , CM000666.1:g.123548080G>C | GRCh37 |
| NC_000004.10:g.123767530G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_104126.1:n.2685+112G>C |