Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14130881C>T , CM000665.2:g.14130881C>T | GRCh38 |
| NC_000003.11:g.14172381C>T , CM000665.1:g.14172381C>T | GRCh37 |
| NC_000003.10:g.14147382C>T | NCBI36 |
| NG_008975.1:g.10942C>T , LRG_435:g.10942C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024334.3:c.222C>T MANE Select | NP_077310.1:p.Pro74= |
| ENST00000306077.5:c.222C>T MANE Select | ENSP00000303992.5:p.Pro74= |
| NM_024334.2:c.222C>T , LRG_435t1:c.222C>T | NP_077310.1:p.Pro74= |
| ENST00000306077.4:c.222C>T | ENSP00000303992.4:p.Pro74= |
| ENST00000432444.1:c.*252C>T | ENSP00000395617.1:n.*252C>T |
| ENST00000432444.2:c.*252C>T | ENSP00000395617.1:n.*252C>T |
| XM_011534109.1:c.117C>T | XP_011532411.1:p.Pro39= |
| XM_017007176.2:c.117C>T | XP_016862665.1:p.Pro39= |