Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71030551T>C , CM000666.2:g.71030551T>C | GRCh38 |
| NC_000004.11:g.71896268T>C , CM000666.1:g.71896268T>C | GRCh37 |
| NC_000004.10:g.72115132T>C | NCBI36 |
| NG_023303.1:g.42004T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286648.10:c.*1173T>C MANE Select | ENSP00000286648.5:n.*1173T>C | |
| ENST00000286648.9:c.*1173T>C | ENSP00000286648.5:n.*1173T>C | |
| ENST00000503359.5:c.*1900T>C | ENSP00000426389.1:n.*1900T>C | |
| ENST00000504730.5:c.*1240T>C | ENSP00000425578.1:n.*1240T>C | |
| ENST00000504952.1:c.*1099T>C | ENSP00000421508.1:n.*1099T>C | |
| NM_000788.2:c.*1173T>C | NP_000779.1:n.*1173T>C | |
| NM_000788.3:c.*1173T>C MANE Select | NP_000779.1:n.*1173T>C |