Linked Data
dbSNP Id:
rs576630476
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.73679785A>G , CM000678.2:g.73679785A>G | GRCh38 |
| NC_000016.9:g.73713684A>G , CM000678.1:g.73713684A>G | GRCh37 |
| NC_000016.8:g.72271185A>G | NCBI36 |
| NG_013211.2:g.217147T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641018.1:n.556T>C | ||
| ENST00000641206.2:c.-1547+395T>C | ENSP00000493252.1:n.-1547+395T>C | |
| ENST00000642085.1:n.163+395T>C | ||
| XR_933730.1:n.355+395T>C | ||
| XM_024450275.1:c.-494+395T>C | XP_024306043.1:n.-494+395T>C | |
| NM_001386735.1:c.-1064+395T>C | NP_001373664.1:n.-1064+395T>C |