Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1612549C>T , CM000668.2:g.1612549C>T | GRCh38 |
| NC_000006.11:g.1612784C>T , CM000668.1:g.1612784C>T | GRCh37 |
| NC_000006.10:g.1557783C>T | NCBI36 |
| NG_009368.1:g.7104C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.*442C>T MANE Select | ENSP00000493906.1:n.*442C>T | |
| ENST00000380874.3:c.*442C>T | ENSP00000370256.2:n.*442C>T | |
| NM_001453.2:c.2104C>T | NP_001444.2:n.2104C>T | |
| NM_001453.3:c.*442C>T MANE Select | NP_001444.2:n.*442C>T |