Linked Data
dbSNP Id:
rs764311408
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928884G>C , CM000684.2:g.43928884G>C | GRCh38 |
| NC_000022.10:g.44324764G>C , CM000684.1:g.44324764G>C | GRCh37 |
| NC_000022.9:g.42656097G>C | NCBI36 |
| NG_008631.1:g.10146G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.481G>C MANE Select | ENSP00000216180.3:p.Gly161Arg | |
| ENST00000216180.7:c.481G>C | ENSP00000216180.3:p.Gly161Arg | |
| ENST00000406117.6:c.*113G>C | ENSP00000384668.2:n.*113G>C | |
| ENST00000423180.2:c.469G>C | ENSP00000397987.2:p.Gly157Arg | |
| ENST00000478713.1:n.515G>C | ||
| NM_025225.2:c.481G>C | NP_079501.2:p.Gly161Arg | |
| NM_025225.3:c.481G>C MANE Select | NP_079501.2:p.Gly161Arg |