Linked Data
gnomAD v4:
8-19951883-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951883C>T , CM000670.2:g.19951883C>T | GRCh38 |
| NC_000008.10:g.19809394C>T , CM000670.1:g.19809394C>T | GRCh37 |
| NC_000008.9:g.19853674C>T | NCBI36 |
| NG_008855.1:g.17813C>T | |
| NG_008855.2:g.55167C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.364C>T MANE Select | ENSP00000497642.1:p.Pro122Ser | |
| ENST00000311322.8:c.364C>T | ENSP00000309757.6:p.Pro122Ser | |
| ENST00000520959.5:c.136C>T | ENSP00000428496.1:p.Pro46Ser | |
| ENST00000524029.5:c.364C>T | ENSP00000428237.1:p.Pro122Ser | |
| NM_000237.2:c.364C>T | NP_000228.1:p.Pro122Ser | |
| NM_000237.3:c.364C>T MANE Select | NP_000228.1:p.Pro122Ser |