Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189005377G>A , CM000664.2:g.189005377G>A | GRCh38 |
| NC_000002.11:g.189870103G>A , CM000664.1:g.189870103G>A | GRCh37 |
| NC_000002.10:g.189578348G>A | NCBI36 |
| NG_007404.1:g.36005G>A , LRG_3:g.36005G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000090.4:c.2959G>A MANE Select | NP_000081.2:p.Gly987Ser |
| ENST00000304636.9:c.2959G>A MANE Select | ENSP00000304408.4:p.Gly987Ser |
| NM_000090.3:c.2959G>A , LRG_3t1:c.2959G>A | NP_000081.1:p.Gly987Ser |
| ENST00000304636.7:c.2959G>A | ENSP00000304408.3:p.Gly987Ser |
| ENST00000317840.9:c.2527+2341G>A | ENSP00000315243.6:n.2527+2341G>A |
| ENST00000450867.2:c.2860G>A | ENSP00000415346.2:p.Gly954Ser |