Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659128G>A , CM000685.2:g.136659128G>A | GRCh38 |
| NC_000023.10:g.135741287G>A , CM000685.1:g.135741287G>A | GRCh37 |
| NC_000023.9:g.135568953G>A | NCBI36 |
| NG_007280.1:g.15952G>A , LRG_141:g.15952G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000074.3:c.499G>A MANE Select | NP_000065.1:p.Gly167Arg |
| ENST00000370629.7:c.499G>A MANE Select | ENSP00000359663.2:p.Gly167Arg |
| NM_000074.2:c.499G>A , LRG_141t1:c.499G>A | NP_000065.1:p.Gly167Arg |
| ENST00000370628.2:c.436G>A | ENSP00000359662.2:p.Gly146Arg |
| ENST00000370629.6:c.499G>A | ENSP00000359663.2:p.Gly167Arg |
| ENST00000695724.1:c.*117G>A | ENSP00000512122.1:n.*117G>A |
| ENST00000695725.1:c.*54G>A | ENSP00000512123.1:n.*54G>A |
| ENST00000695726.1:n.2467G>A | |
| ENST00000695729.1:n.3302G>A |