Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119422901C>T , CM000663.2:g.119422901C>T | GRCh38 |
| NC_000001.10:g.119965524C>T , CM000663.1:g.119965524C>T | GRCh37 |
| NC_000001.9:g.119767047C>T | NCBI36 |
| NG_013349.1:g.12971C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.*281C>T MANE Select | ENSP00000358424.3:n.*281C>T | |
| ENST00000369416.3:c.*281C>T | ENSP00000358424.3:n.*281C>T | |
| ENST00000543831.5:c.*281C>T | ENSP00000445122.1:n.*281C>T | |
| NM_000198.3:c.*281C>T | NP_000189.1:n.*281C>T | |
| NM_001166120.1:c.*281C>T | NP_001159592.1:n.*281C>T | |
| NM_000198.4:c.*281C>T MANE Select | NP_000189.1:n.*281C>T | |
| NM_001166120.2:c.*281C>T | NP_001159592.1:n.*281C>T |