Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52451410G>A , CM000665.2:g.52451410G>A | GRCh38 |
| NC_000003.11:g.52485426G>A , CM000665.1:g.52485426G>A | GRCh37 |
| NC_000003.10:g.52460466G>A | NCBI36 |
| NG_008963.1:g.7632C>T , LRG_378:g.7632C>T | |
| NG_033112.1:g.903G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003280.3:c.435C>T MANE Select | NP_003271.1:p.Asp145= |
| ENST00000232975.8:c.435C>T MANE Select | ENSP00000232975.3:p.Asp145= |
| NM_003280.2:c.435C>T , LRG_378t1:c.435C>T | NP_003271.1:p.Asp145= |
| ENST00000232975.7:c.435C>T | ENSP00000232975.3:p.Asp145= |