Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812352T>C , CM000672.2:g.110812352T>C | GRCh38 |
| NC_000010.10:g.112572110T>C , CM000672.1:g.112572110T>C | GRCh37 |
| NC_000010.9:g.112562100T>C | NCBI36 |
| NG_021177.1:g.172956T>C , LRG_382:g.172956T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.1955T>C MANE Select | ENSP00000358532.3:p.Phe652Ser | |
| ENST00000369519.3:c.1955T>C | ENSP00000358532.3:p.Phe652Ser | |
| NM_001134363.2:c.1955T>C | NP_001127835.2:p.Phe652Ser | |
| XM_011539697.1:c.1571T>C | XP_011537999.1:p.Phe524Ser | |
| XM_017016103.2:c.1790T>C | XP_016871592.1:p.Phe597Ser | |
| XM_017016104.2:c.1571T>C | XP_016871593.1:p.Phe524Ser | |
| NM_001134363.3:c.1955T>C MANE Select | NP_001127835.2:p.Phe652Ser |