Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52452167C>A , CM000665.2:g.52452167C>A | GRCh38 |
| NC_000003.11:g.52486183C>A , CM000665.1:g.52486183C>A | GRCh37 |
| NC_000003.10:g.52461223C>A | NCBI36 |
| NG_008963.1:g.6875G>T , LRG_378:g.6875G>T | |
| NG_033112.1:g.1660C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003280.3:c.141G>T MANE Select | NP_003271.1:p.Met47Ile |
| ENST00000232975.8:c.141G>T MANE Select | ENSP00000232975.3:p.Met47Ile |
| NM_003280.2:c.141G>T , LRG_378t1:c.141G>T | NP_003271.1:p.Met47Ile |
| ENST00000232975.7:c.141G>T | ENSP00000232975.3:p.Met47Ile |
| ENST00000496590.1:c.9G>T | ENSP00000420596.1:p.Met3Ile |