Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52452117A>G , CM000665.2:g.52452117A>G | GRCh38 |
| NC_000003.11:g.52486133A>G , CM000665.1:g.52486133A>G | GRCh37 |
| NC_000003.10:g.52461173A>G | NCBI36 |
| NG_008963.1:g.6925T>C , LRG_378:g.6925T>C | |
| NG_033112.1:g.1610A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000232975.8:c.191T>C MANE Select | ENSP00000232975.3:p.Val64Ala | |
| ENST00000232975.7:c.191T>C | ENSP00000232975.3:p.Val64Ala | |
| ENST00000496590.1:c.59T>C | ENSP00000420596.1:p.Val20Ala | |
| NM_003280.2:c.191T>C , LRG_378t1:c.191T>C | NP_003271.1:p.Val64Ala | |
| NM_003280.3:c.191T>C MANE Select | NP_003271.1:p.Val64Ala |