Linked Data
dbSNP Id:
rs1029618165
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403459C>T , CM000673.2:g.130403459C>T | GRCh38 |
| NC_000011.9:g.130273354C>T , CM000673.1:g.130273354C>T | GRCh37 |
| NC_000011.8:g.129778564C>T | NCBI36 |
| NG_052870.1:g.30535G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2554C>T | ||
| XR_948178.1:n.2208C>T | ||
| XR_948179.1:n.2126C>T | ||
| XR_948180.1:n.2126C>T | ||
| XR_948181.1:n.695C>T | ||
| XR_948182.1:n.2286C>T | ||
| XR_948183.1:n.458+9660C>T | ||
| XR_948184.1:n.617C>T | ||
| XR_948185.1:n.546C>T | ||
| XR_948187.1:n.458+9660C>T | ||
| XR_948188.1:n.449C>T | ||
| XR_948189.1:n.497C>T | ||
| NR_148980.1:n.770C>T |