Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665999G>A , CM000663.2:g.172665999G>A | GRCh38 |
| NC_000001.10:g.172635139G>A , CM000663.1:g.172635139G>A | GRCh37 |
| NC_000001.9:g.170901762G>A | NCBI36 |
| NG_007269.1:g.11955G>A , LRG_58:g.11955G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000639.3:c.829G>A MANE Select | NP_000630.1:p.Gly277Ser |
| ENST00000367721.3:c.829G>A MANE Select | ENSP00000356694.2:p.Gly277Ser |
| NM_000639.2:c.829G>A | NP_000630.1:p.Gly277Ser |
| NM_001302746.1:c.*399G>A | NP_001289675.1:n.*399G>A |
| NM_001302746.2:c.*399G>A | NP_001289675.1:n.*399G>A |
| ENST00000340030.4:c.*399G>A | ENSP00000344739.3:n.*399G>A |
| ENST00000367721.2:c.829G>A | ENSP00000356694.2:p.Gly277Ser |