Linked Data
gnomAD v4:
10-110812429-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812429C>T , CM000672.2:g.110812429C>T | GRCh38 |
| NC_000010.10:g.112572187C>T , CM000672.1:g.112572187C>T | GRCh37 |
| NC_000010.9:g.112562177C>T | NCBI36 |
| NG_021177.1:g.173033C>T , LRG_382:g.173033C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.2032C>T MANE Select | ENSP00000358532.3:p.His678Tyr | |
| ENST00000369519.3:c.2032C>T | ENSP00000358532.3:p.His678Tyr | |
| NM_001134363.2:c.2032C>T | NP_001127835.2:p.His678Tyr | |
| XM_011539697.1:c.1648C>T | XP_011537999.1:p.His550Tyr | |
| XM_017016103.2:c.1867C>T | XP_016871592.1:p.His623Tyr | |
| XM_017016104.2:c.1648C>T | XP_016871593.1:p.His550Tyr | |
| NM_001134363.3:c.2032C>T MANE Select | NP_001127835.2:p.His678Tyr |