Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55063588C>T , CM000663.2:g.55063588C>T | GRCh38 |
| NC_000001.10:g.55529261C>T , CM000663.1:g.55529261C>T | GRCh37 |
| NC_000001.9:g.55301849C>T | NCBI36 |
| NG_009061.1:g.29042C>T , LRG_275:g.29042C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*423C>T | ENSP00000501161.2:n.*423C>T | |
| ENST00000710286.1:c.*4C>T | ENSP00000518176.1:n.*4C>T | |
| ENST00000673903.1:c.*4C>T | ENSP00000501257.1:n.*4C>T | |
| ENST00000302118.5:c.*4C>T MANE Select | ENSP00000303208.5:n.*4C>T | |
| ENST00000490692.1:n.2629C>T | ||
| NM_174936.3:c.*4C>T , LRG_275t1:c.*4C>T | NP_777596.2:n.*4C>T | |
| NR_110451.1:n.1690C>T | ||
| XM_011541193.1:c.*4C>T | XP_011539495.1:n.*4C>T | |
| NM_174936.4:c.*4C>T MANE Select | NP_777596.2:n.*4C>T | |
| NR_110451.2:n.1690C>T |