Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827487A>C , CM000667.2:g.148827487A>C | GRCh38 |
| NC_000005.9:g.148207050A>C , CM000667.1:g.148207050A>C | GRCh37 |
| NC_000005.8:g.148187243A>C | NCBI36 |
| NG_016421.1:g.5895A>C | |
| NG_016421.2:g.5895A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.656A>C MANE Select | ENSP00000305372.4:p.Tyr219Ser | |
| ENST00000305988.5:c.656A>C | ENSP00000305372.4:p.Tyr219Ser | |
| NM_000024.5:c.656A>C | NP_000015.1:p.Tyr219Ser | |
| NM_000024.6:c.656A>C MANE Select | NP_000015.2:p.Tyr219Ser |