Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94055122T>C , CM000663.2:g.94055122T>C | GRCh38 |
| NC_000001.10:g.94520678T>C , CM000663.1:g.94520678T>C | GRCh37 |
| NC_000001.9:g.94293266T>C | NCBI36 |
| NG_009073.1:g.71028A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.2576A>G MANE Select | NP_000341.2:p.Gln859Arg |
| ENST00000370225.4:c.2576A>G MANE Select | ENSP00000359245.3:p.Gln859Arg |
| NM_000350.2:c.2576A>G | NP_000341.2:p.Gln859Arg |
| ENST00000370225.3:c.2576A>G | ENSP00000359245.3:p.Gln859Arg |
| ENST00000536513.5:c.-65+8052A>G | ENSP00000439707.2:n.-65+8052A>G |
| ENST00000649773.1:c.2354A>G | ENSP00000496882.1:p.Gln785Arg |