Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52451819A>G , CM000665.2:g.52451819A>G | GRCh38 |
| NC_000003.11:g.52485835A>G , CM000665.1:g.52485835A>G | GRCh37 |
| NC_000003.10:g.52460875A>G | NCBI36 |
| NG_008963.1:g.7223T>C , LRG_378:g.7223T>C | |
| NG_033112.1:g.1312A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000232975.8:c.242T>C MANE Select | ENSP00000232975.3:p.Met81Thr | |
| ENST00000232975.7:c.242T>C | ENSP00000232975.3:p.Met81Thr | |
| ENST00000461086.1:n.173T>C | ||
| ENST00000496590.1:c.110T>C | ENSP00000420596.1:p.Met37Thr | |
| NM_003280.2:c.242T>C , LRG_378t1:c.242T>C | NP_003271.1:p.Met81Thr | |
| NM_003280.3:c.242T>C MANE Select | NP_003271.1:p.Met81Thr |