Linked Data
dbSNP Id:
rs281860652
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176929G>C , CM000678.2:g.176929G>C | GRCh38 |
| NC_000016.9:g.226928G>C , CM000678.1:g.226928G>C | GRCh37 |
| NC_000016.8:g.166928G>C | NCBI36 |
| NG_000006.1:g.37792G>C | |
| NG_059186.1:g.5279G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.96G>C MANE Select | ENSP00000322421.5:p.Arg32Ser | |
| ENST00000397797.1:c.-1G>C | ENSP00000380899.1:n.-1G>C | |
| ENST00000472694.1:n.232G>C | ||
| ENST00000487791.1:n.65G>C | ||
| NM_000558.4:c.96G>C | NP_000549.1:p.Arg32Ser | |
| NM_000558.5:c.96G>C MANE Select | NP_000549.1:p.Arg32Ser |