Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14129509T>C , CM000665.2:g.14129509T>C | GRCh38 |
| NC_000003.11:g.14171009T>C , CM000665.1:g.14171009T>C | GRCh37 |
| NC_000003.10:g.14146010T>C | NCBI36 |
| NG_008975.1:g.9570T>C , LRG_435:g.9570T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*140T>C | ENSP00000395617.1:n.*140T>C | |
| ENST00000306077.5:c.110T>C MANE Select | ENSP00000303992.5:p.Phe37Ser | |
| ENST00000306077.4:c.110T>C | ENSP00000303992.4:p.Phe37Ser | |
| ENST00000432444.1:c.*140T>C | ENSP00000395617.1:n.*140T>C | |
| NM_024334.2:c.110T>C , LRG_435t1:c.110T>C | NP_077310.1:p.Phe37Ser | |
| XM_011534109.1:c.5T>C | XP_011532411.1:p.Phe2Ser | |
| XM_017007176.2:c.5T>C | XP_016862665.1:p.Phe2Ser | |
| NM_024334.3:c.110T>C MANE Select | NP_077310.1:p.Phe37Ser |