Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189098735C>G , CM000664.2:g.189098735C>G | GRCh38 |
| NC_000002.11:g.189963461C>G , CM000664.1:g.189963461C>G | GRCh37 |
| NC_000002.10:g.189671706C>G | NCBI36 |
| NG_011799.1:g.86145G>C | |
| NG_011799.2:g.86145G>C | |
| NG_011799.3:g.131567G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.394G>C MANE Select | ENSP00000364000.3:p.Gly132Arg | |
| ENST00000649966.1:c.256G>C | ENSP00000496785.1:p.Gly86Arg | |
| ENST00000374866.7:c.394G>C | ENSP00000364000.3:p.Gly132Arg | |
| ENST00000618828.1:c.-237G>C | ENSP00000482184.1:n.-237G>C | |
| NM_000393.3:c.394G>C | NP_000384.2:p.Gly132Arg | |
| XM_011510573.1:c.256G>C | XP_011508875.1:p.Gly86Arg | |
| NM_000393.4:c.394G>C | NP_000384.2:p.Gly132Arg | |
| XM_011510573.3:c.256G>C | XP_011508875.1:p.Gly86Arg | |
| NM_000393.5:c.394G>C MANE Select | NP_000384.2:p.Gly132Arg |