Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52452266T>G , CM000665.2:g.52452266T>G | GRCh38 |
| NC_000003.11:g.52486282T>G , CM000665.1:g.52486282T>G | GRCh37 |
| NC_000003.10:g.52461322T>G | NCBI36 |
| NG_008963.1:g.6776A>C , LRG_378:g.6776A>C | |
| NG_033112.1:g.1759T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003280.3:c.56-14A>C MANE Select | NP_003271.1:n.56-14A>C |
| ENST00000232975.8:c.56-14A>C MANE Select | ENSP00000232975.3:n.56-14A>C |
| NM_003280.2:c.56-14A>C , LRG_378t1:c.56-14A>C | NP_003271.1:n.56-14A>C |
| ENST00000232975.7:c.56-14A>C | ENSP00000232975.3:n.56-14A>C |
| ENST00000496590.1:c.-77-14A>C | ENSP00000420596.1:n.-77-14A>C |