Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52451399T= , CM000665.2:g.52451399T= | GRCh38 |
| NC_000003.11:g.52485415T= , CM000665.1:g.52485415T= | GRCh37 |
| NC_000003.10:g.52460455T= | NCBI36 |
| NG_008963.1:g.7643A= , LRG_378:g.7643A= | |
| NG_033112.1:g.892T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003280.3:c.446A= MANE Select | NP_003271.1:p.Asp149= |
| ENST00000232975.8:c.446A= MANE Select | ENSP00000232975.3:p.Asp149= |
| NM_003280.2:c.446A= , LRG_378t1:c.446A= | NP_003271.1:p.Asp149= |
| ENST00000232975.7:c.446A= | ENSP00000232975.3:p.Asp149= |